# recalling — RSS Amplifier

Recent posts from the 3 feeds in the RSS Amplifier directory that cover recalling.

Page: <https://rssamplifier.com/topics/recalling>  
Feed: <https://rssamplifier.com/topics/recalling.md>

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## [Updated – Dreyer’s Grand Ice Cream, Inc. Issues Voluntary Recall on Select Outshine Fruit Bars Due to Possible Foreign Matter Contamination](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-dreyers-grand-ice-cream-inc-issues-voluntary-recall-select-outshine-fruit-bars-due-possible)

_2026-08-18 · FDA · FDA Food Safety Recalls RSS Feed_

August 18, 2026 - Dreyer’s Grand Ice Cream, Inc. is voluntarily recalling a limited number of select flavors of Outshine Fruit Bars due to possible foreign material contamination with glass. Products affected include Outshine Strawberry, Watermelon, Grape, Tangerine and Black Cherry 6-Count 2.5 ounc

## [Early Alert: Convenience Kit Issue from Becton Dickinson](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-convenience-kit-issue-becton-dickinson)

_2026-08-18 · FDA · MedWatch Safety Alerts RSS Feed_

BD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampules

## [L-Nutra Issues Allergy Alert on Undeclared Tree Nuts in Prolon Brand Apulian Almond & Cocoa Spread](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/l-nutra-issues-allergy-alert-undeclared-tree-nuts-prolon-brand-apulian-almond-cocoa-spread)

_2026-08-18 · FDA · FDA Food Safety Recalls RSS Feed_

L-Nutra of Culver City, California is recalling Prolon brand Apulian Almond & Cocoa Spread because it contains undeclared cashew, pistachio, and hazelnut. People who have an allergy or severe sensitivity to cashew, pistachio, and/or hazelnut run the risk of serious or life-threatening allergic react

## [UPDATED: Oma's Pride Voluntarily Recalls One Lot of Woof Complete Canine Chicken Recipe (6 Lb Bag) Because of Possible Salmonella Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-omas-pride-voluntarily-recalls-one-lot-woof-complete-canine-chicken-recipe-6-lb-bag-because)

_2026-08-17 · FDA · FDA Food Safety Recalls RSS Feed_

Oma's Pride of Avon, Connecticut, is voluntarily recalling one lot of Woof Complete Canine Chicken Recipe, 6 lb bag (Lot BB012729) because it is contaminated with Salmonella.

## [Intraosseous Needle Set Recall: Becton Dickinson Removes Certain Intraosseous Vascular Access System Needle Sets](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/intraosseous-needle-set-recall-becton-dickinson-removes-certain-intraosseous-vascular-access-system)

_2026-08-17 · FDA · MedWatch Safety Alerts RSS Feed_

BD is recalling certain BD Intraosseous Vascular Access System Needle Sets due to difficulty removing the obturator (stylet) following placement.

## [The Hampton Grocers, Inc . Recalls It’s 8 Ounce Packages of “Lacnola Lactation Granola” Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hampton-grocers-inc-recalls-its-8-ounce-packages-lacnola-lactation-granola-because-possible-health)

_2026-08-14 · FDA · FDA Food Safety Recalls RSS Feed_

The Hampton Grocers, Inc. of Montauk, NY is recalling Lacnola Lactation Granola, 8oz, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune system

## [Grand Central Bakery Recalls Potato Sourdough Bread Due to Possible Foreign Object](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/grand-central-bakery-recalls-potato-sourdough-bread-due-possible-foreign-object)

_2026-08-13 · FDA · FDA Food Safety Recalls RSS Feed_

August 12, 2026, Grand Central Bakery of Seattle, WA is recalling loaves of Potato Sourdough because they may contain the presence of pieces of metal.

## [Intravascular Administration Set Recall: Baxter Removes Duo-Vent Solution Sets](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/intravascular-administration-set-recall-baxter-removes-duo-vent-solution-sets)

_2026-08-13 · FDA · MedWatch Safety Alerts RSS Feed_

Baxter administration sets may have air bubbles in the drip chamber and tubing, which may result in air being delivered through the IV line to the patient.

## [Kettle Cuisine Recalls Marketside Tomato Bisque Soup Kit – Sold Exclusively at Walmart Stores Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kettle-cuisine-recalls-marketside-tomato-bisque-soup-kit-sold-exclusively-walmart-stores-because)

_2026-08-12 · FDA · FDA Food Safety Recalls RSS Feed_

Kettle Cuisine LLC of Savage, MD is recalling Marketside Tomato Bisque Soup Kit – 14oz (397g) because the product has the potential to be contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others

## [Hardie’s Fresh Foods Recalls Jalapenos Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hardies-fresh-foods-recalls-jalapenos-because-possible-health-risk)

_2026-08-12 · FDA · FDA Food Safety Recalls RSS Feed_

Dairyland Produce, LLC, dba Hardie’s Fresh Foods of Houston, TX and Dallas, TX are recalling PEPPER JALAPENO 5#, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others

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## [Whole Foods Market Announces a Recall of Select Salsas, Guacamole, Pico de Gallo, and Prepared Foods Products Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-announces-recall-select-salsas-guacamole-pico-de-gallo-and-prepared-foods)

_2026-08-12 · FDA · FDA Food Safety Recalls RSS Feed_

AUSTIN, Texas — Whole Foods Market is recalling select products from its Produce and Prepared Foods departments that contain jalapeños sourced from Coast Citrus Distributors due to potential Salmonella contamination. Salmonella is an organism which can cause serious and sometimes fatal infections in

## [Update on Alert: Convenience Kit Issue from Medline](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/update-alert-convenience-kit-issue-medline)

_2026-08-12 · FDA · MedWatch Safety Alerts RSS Feed_

Certain BD ChloraPrep Applicators in Convenience Kits manufactured by Medline may not be sterile.

## [Convenience Kit Correction: Medline Issues Correction for Convenience Kits Containing ICU Medical Pain Management Components](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/convenience-kit-correction-medline-issues-correction-convenience-kits-containing-icu-medical-pain)

_2026-08-12 · FDA · MedWatch Safety Alerts RSS Feed_

Medline is correcting affected convenience kits by removing included ICU Medical pain management components containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP.

## [Recall of Jalapeno Avocado Dressing Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/recall-jalapeno-avocado-dressing-because-possible-health-risk)

_2026-08-11 · FDA · FDA Food Safety Recalls RSS Feed_

HOUSTON, TX (August 11, 2026) – Salata Dressings of Houston, TX, is recalling its Jalapeno Avocado Dressing because it had the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with

## [Lidl US Recalls Vitasia Asian Style Wok Spice Mix Due to Potential Salmonella Contamination](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lidl-us-recalls-vitasia-asian-style-wok-spice-mix-due-potential-salmonella-contamination)

_2026-08-11 · FDA · FDA Food Safety Recalls RSS Feed_

ARLINGTON, VA – AUGUST 11, 2026 – Lidl US is recalling one lot of Vitasia Asian Style Wok Spice Mix 1.58 oz (45g) (UPC 4335619355491) with Lot # 155846 and BBD JUN 2028 because it has the potential to be contaminated with Salmonella.

## [Henkel Corp. Announces a Nationwide Recall of Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml Due to Packaging Imperfection](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/henkel-corp-announces-nationwide-recall-schwarzkopf-professional-osis-grip-676-fl-oz200-ml-due)

_2026-08-11 · FDA · Food and Drugs Administration--Recalls/Safety Alerts_

Rocky Hill, CT -- Henkel Corporation (“Henkel”) is voluntarily recalling its Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml sold in the United States due to a potential packaging issue in which product could leak from the package under pressure, which creates a risk of explosion.

## [Frankie's Organic Issues Allergy Alert on Undeclared Milk in Frankie’s Organic Plant-Based Vegan Cheddar Puffs](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frankies-organic-issues-allergy-alert-undeclared-milk-frankies-organic-plant-based-vegan-cheddar)

_2026-08-11 · FDA · FDA Food Safety Recalls RSS Feed_

Laval, Quebec Frankie's Organic is recalling 94 cases of Frankie’s Organic Plant-Based Vegan Cheddar Puffs because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

## [Breathing Circuit Set Recall: Hamilton Medical Removes Breathing Circuit Set](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/breathing-circuit-set-recall-hamilton-medical-removes-breathing-circuit-set)

_2026-08-11 · FDA · MedWatch Safety Alerts RSS Feed_

The ventilator breathing circuits are intended to connect a ventilator to a patient tube or mask. Obstruction may result in inadequate ventilation.

## [Fresenius Kabi Issues Nationwide Recall of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL Vials Due to Presence of Glass Particles](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-nationwide-recall-tyenner-tocilizumab-aazg-injection-400-mg20-ml-vials-due)

_2026-08-11 · FDA · MedWatch Safety Alerts RSS Feed_

FOR IMMEDIATE RELEASE – August 10, 2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is recalling one lot of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL (20 mg/mL)20 mL vials to the user level. An internal investigation at the firm found the product to cont

## [Catheter Introducer Correction: Abiomed and Oscor Issue Correction for Catheter Introducer](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/catheter-introducer-correction-abiomed-and-oscor-issue-correction-catheter-introducer)

_2026-08-10 · FDA · MedWatch Safety Alerts RSS Feed_

Abiomed and Oscor have identified a potential for introducer sheath leakage in 14Fr and 23Fr Introducers that may increase the risk of access-site bleeding.

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## [Taylor Fresh Foods Recalls Products Made with Jalapeno Peppers Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/taylor-fresh-foods-recalls-products-made-jalapeno-peppers-because-possible-health-risk)

_2026-08-09 · FDA · FDA Food Safety Recalls RSS Feed_

Salinas, Calif., August 9, 2026 – Upon notification that Coast Citrus Distributors is voluntarily recalling fresh jalapeños due to potential Salmonella contamination, Taylor Fresh Foods is recalling finished products containing jalapeños subject to this recall.Salmonella, an organism which can cause

## [NatureBest Precut & Produce LLC Voluntarily Recalls Products Containing Jalapenos Due to Potential Salmonella Contamination](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/naturebest-precut-produce-llc-voluntarily-recalls-products-containing-jalapenos-due-potential)

_2026-08-08 · FDA · FDA Food Safety Recalls RSS Feed_

NatureBest Precut & Produce LLC, with facilities located in Missouri City, TX and Houston, TX is voluntarily recalling products containing jalapeño peppers supplied by Coast Citrus Distributors due to the potential for contamination with Salmonella. Salmonella is an organism which can cause serious

## [Lexunder Inc Recalls Food to Live Brand Green Powder Products Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lexunder-inc-recalls-food-live-brand-green-powder-products-because-possible-health-risk)

_2026-08-07 · FDA · FDA Food Safety Recalls RSS Feed_

Lexunder Inc., doing business as Food To Live of Brooklyn, NY, is recalling Food to Live brand green powder products because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and

## [Medline Industries, LP Issues Nationwide Recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-hudson-rci-neonatalinfant-heated-wire-breathing)

_2026-08-06 · FDA · MedWatch Safety Alerts RSS Feed_

On July 13, 2026, Medline Industries, LP initiated a nationwide recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits. Medline received reports of sporadic failures involving the electrical connector of certain neonatal and infant heated wire breathing circuits. In affected circuits, t

## [Victory Medical Center Pharmacy Issues Voluntary Nationwide Recall of Certain Lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials Due to Elevated Endotoxin Levels](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/victory-medical-center-pharmacy-issues-voluntary-nationwide-recall-certain-lots-compounded)

_2026-08-05 · FDA · Food and Drugs Administration--Recalls/Safety Alerts_

FOR IMMEDIATE RELEASE – August 5, 2026 – Austin, Texas, Victory Medical Center Pharmacy is voluntarily recalling certain lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials to the patient level. The product is being recalled because pharmacy testing identified elevated bacterial endotoxin leve

## [Sun Noodle Issues Voluntary Recall of Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base Due to Undeclared Fish Allergen](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sun-noodle-issues-voluntary-recall-sura-tanmen-hot-and-sour-flavor-premium-japanese-noodles-soup)

_2026-08-05 · FDA · FDA Food Safety Recalls RSS Feed_

August 5, 2026 — Sun Noodle of Honolulu, Hawaii is voluntarily recalling 134 packages (15.4oz) of Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base, because the product may contain undeclared fish allergen. People who have an allergy or severe sensitivity to fish run the risk of a

## [Fresenius Kabi Issues Voluntary Nationwide Recall of One Lot of Morphine Sulfate Injection, USP in a Simplist® Prefilled Syringe Due to Labeling Mix-up](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-one-lot-morphine-sulfate-injection-usp-simplistr)

_2026-08-05 · FDA · MedWatch Safety Alerts RSS Feed_

FOR IMMEDIATE RELEASE – 8/4/2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is voluntarily recalling one lot of Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL due to a label mix-up. The MicroVault labeled as Morphine 2 mg/1 mL, may contain a Prefilled Syri

## [Blank Slate Creamery Issues Allergy Alert on Undeclared Egg in Vegan Non-Dairy Frozen Dessert Coconut Fudge Sandwiches](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/blank-slate-creamery-issues-allergy-alert-undeclared-egg-vegan-non-dairy-frozen-dessert-coconut)

_2026-08-04 · FDA · FDA Food Safety Recalls RSS Feed_

Blank Slate Creamery of Ann Arbor, MI is recalling its 4.5 oz. packaged VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, because it may contain undeclared egg. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consu

## [Liebel-Flarsheim Company, LLC Issues Recall of OPTIRAY Imaging Bulk Package - 350, 500mL, Vial, Nationwide and Mexico Due to Presence of Particulate Matter](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/liebel-flarsheim-company-llc-issues-recall-optiray-imaging-bulk-package-350-500ml-vial-nationwide)

_2026-08-04 · FDA · MedWatch Safety Alerts RSS Feed_

FOR IMMEDIATE RELEASE – July 31, 2026 – Raleigh, North Carolina, Liebel-Flarsheim Company, LLC, is recalling one lot of OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial, (Ioversol Injection 74% 350 mg iodine/ml) for intra-arterial or intra-venous use to the user level (hospitals, imaging center

## [Early Alert: Intraosseous Needle Set Issue from Becton Dickinson](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-intraosseous-needle-set-issue-becton-dickinson)

_2026-08-04 · FDA · MedWatch Safety Alerts RSS Feed_

BD is recalling certain BD Intraosseous Vascular Access System Needle Sets due to difficulty removing the obturator (stylet) following placement.

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## [Boticelli Foods Recalls Bettergoods Pistachio Nut Butter Because of Possible Health Risk](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/boticelli-foods-recalls-bettergoods-pistachio-nut-butter-because-possible-health-risk)

_2026-08-03 · FDA · FDA Food Safety Recalls RSS Feed_

Boticelli Foods of Melville NY, is recalling 1 lot of bettergoods Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961, Lot LB028ACP04, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail

## [Convenience Kit Correction: Medical Action Industries Issues Correction for Kits Containing Recalled Namic Manifolds](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/convenience-kit-correction-medical-action-industries-issues-correction-kits-containing-recalled)

_2026-08-03 · FDA · MedWatch Safety Alerts RSS Feed_

Particulates have the potential to be introduced into blood circulation and become lodged within blood vessels.

## [American Regent, Inc. Animal Health Issues Nationwide Recall of Two Lots of Adequan® Canine and Two Lots of Adequan® I.M. Due to Visible Glass Fiber Material in the Product](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-regent-inc-animal-health-issues-nationwide-recall-two-lots-adequanr-canine-and-two-lots)

_2026-08-03 · FDA · MedWatch Safety Alerts RSS Feed_

FOR IMMEDIATE RELEASE – July 31, 2026 – Shirley, NY, American Regent, Inc. Animal Health is conducting a nationwide recall of two lots (25011 and 3369) of Adequan® Canine Injection (for dogs), 100 mg/mL 5mL multi-dose vials and two lots (24416 and 25265P) of Adequan® i.m. Injection (for horses), 500

## [BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due)

_2026-08-03 · FDA · MedWatch Safety Alerts RSS Feed_

FRANKLIN LAKES, N.J. (July 31, 2026) – BD (Becton, Dickinson and Company) is voluntarily recalling specific lots of BD® Intraosseous Vascular Access System Needle Sets to the user level. These products are being recalled following reports that some users experienced difficulty removing the obturato

## [Convenience Kit Correction: Medline Issues Correction for Kits Containing Huons Lidocaine Hydrochloride and Bupivacaine Hydrochloride in Dextrose Injection](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/convenience-kit-correction-medline-issues-correction-kits-containing-huons-lidocaine-hydrochloride)

_2026-08-03 · FDA · MedWatch Safety Alerts RSS Feed_

Medline is correcting affected convenience kits by removing recalled Lidocaine Hydrochloride and Bupivacaine Hydrochloride in Dextrose Injection components from affected convenience kits.

## [Lidl US Expands Recall of Eridanous Shortbread Cookies Due to Undeclared Wheat, Soy, Milk, Egg and Tree Nut (Coconut) Allergens](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lidl-us-expands-recall-eridanous-shortbread-cookies-due-undeclared-wheat-soy-milk-egg-and-tree-nut)

_2026-07-31 · FDA · FDA Food Safety Recalls RSS Feed_

ARLINGTON, VA – JULY 31, 2026 – Lidl US is expanding its July 24, 2026 recall of Eridanous Shortbread Cookies to include all units with a foreign language ingredients and nutrition facts panel for the following products:

## [Ventilator Correction: Resmed Issues Correction for Astral Ventilator](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/ventilator-correction-resmed-issues-correction-astral-ventilator)

_2026-07-31 · FDA · MedWatch Safety Alerts RSS Feed_

Failure of an electrical component in certain Astral ventilators may cause an interruption or failure in therapy which may result in serious injury or death.

## [Catheter Introducer Kit Recall: Abiomed Removes 14Fr Low Profile Introducer Kits](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/catheter-introducer-kit-recall-abiomed-removes-14fr-low-profile-introducer-kits)

_2026-07-31 · FDA · MedWatch Safety Alerts RSS Feed_

Prolonged use of the Abiomed 14Fr Low Profile Introducer may lead to thrombus formation.

## [Ukrop’s Homestyle Foods Announces a Voluntary Recall Due to Possible Foreign Object](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ukrops-homestyle-foods-announces-voluntary-recall-due-possible-foreign-object)

_2026-07-30 · FDA · FDA Food Safety Recalls RSS Feed_

Richmond, VA – Ukrop's Homestyle Foods, LLC today is voluntarily recalling six of its products due to the potential presence of a foreign object.

## [Convenience Kit Correction: Argon Medical Issues Correction for Convenience Kits Containing Spectra Medical Device Lidocaine Ampules](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/convenience-kit-correction-argon-medical-issues-correction-convenience-kits-containing-spectra)

_2026-07-30 · FDA · MedWatch Safety Alerts RSS Feed_

Argon Medical is correcting affected convenience kits by removing included Spectra Medical Devices Lidocaine Ampules.

## [Publix Recalls All Lots of GreenWise Organic Frozen Blueberries and Whole Mixed Berries Due to Potential E. coli O145 Contamination](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/publix-recalls-all-lots-greenwise-organic-frozen-blueberries-and-whole-mixed-berries-due-potential-e)

_2026-07-29 · FDA · FDA Food Safety Recalls RSS Feed_

July 29, 2026 ¬— Publix is recalling all lots of GreenWise Organic Whole Blueberries and Whole Mixed Berries because they may be contaminated with Escherichia coli O145:H28 (E. coli O145). E. coli O145 is a Shiga toxin-producing E. coli (STEC) that can cause illness characterized by severe stomach c

## [529 Commerce LLC Recalls Rooted in Rare Brand Aquafaba Powder Due to Undeclared Eggs](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/529-commerce-llc-recalls-rooted-rare-brand-aquafaba-powder-due-undeclared-eggs)

_2026-07-29 · FDA · FDA Food Safety Recalls RSS Feed_

529 Commerce, LLC of Parkland, Florida is recalling 3,860 units of its 4oz and 12 oz packages of its Rooted in Rare brand Aquafaba Powder because the product may contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reac

## [American Regent, Inc. Issues Voluntary Nationwide Recall of One Lot of Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL Due to the Presence of Visible Particulate Matter](http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-regent-inc-issues-voluntary-nationwide-recall-one-lot-papaverine-hydrochloride-injection)

_2026-07-27 · FDA · MedWatch Safety Alerts RSS Feed_

July 24, 2026 – Shirley, NY, American Regent, Inc. is conducting a nationwide voluntary recall of a single lot of Papaverine Hydrochloride Injection, USP, 60 mg/2 mL single dose vial to the consumer level. The product is being recalled due to the presence of particulate matter identified as glass an

## [Early Alert: Percutaneous Catheter Issue from Boston Scientific](http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-percutaneous-catheter-issue-boston-scientific)

_2026-07-24 · FDA · MedWatch Safety Alerts RSS Feed_

ENROUTE Transcarotid Neuroprotection Systems may have arterial sheath tip separation or partial tip separation during use

