Back to recall look-up

Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 18 of 1329

Medical devices

Reported Aug 12, 2026

Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems Nederland B.v.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pride Mobility Products Corp.

12 more products in this recall

FDA (openFDA device enforcement)

Reported Aug 12, 2026

Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PT Organics Limited

FDA (openFDA food enforcement)

Reported Aug 12, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rhode Island Blood Center, A Division

FDA (weekly enforcement report)

Medical devices

Reported Aug 12, 2026

Syva Emit Disopyramide Assay Enzyme Immunoassay, Lidocaine SMN 10445370 Catalog No 6N319UL

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Reported Aug 12, 2026

Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sunny Pharmtech Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Reported Aug 12, 2026Updated Sep 16, 2026

Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The American National Red Cross

FDA (weekly enforcement report)

Medical devices

Reported Aug 12, 2026

Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Therabody, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0, App version 7.28.0.11

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Theranica Bioelectronics Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number: NCOCO1510 Software Version: N/A…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tissium Sa

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

United Orthopedic Corp.

5 more products in this recall

FDA (openFDA device enforcement)

Reported Aug 12, 2026Updated Sep 16, 2026

Remedy Recovery Dogswell, Pet Wormer, for dogs, cats, puppies, & kittens, Net Contents 236 ml (8 fl oz), Distributed by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Westwood Laboratories, LLC.

FDA (weekly enforcement report)

Reported Aug 12, 2026Updated Sep 17, 2026

Whole Foods Market recalls Whole Foods Market Finished products such as dips, salsa, guacamole, and more containing jalapeno. due to Potential Salmonella…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Whole Foods Market

FDA (recalls & safety alerts)

Reported Aug 12, 2026

Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Matoda,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zydus Pharmaceuticals (USA) Inc.

FDA (openFDA drug enforcement)

Reported Aug 11, 2026Updated Sep 17, 2026

Fresenius Kabi recalls Fresenius Kabi Tyenne Injection 400 mg/20 mL vial due to Due to Presence of Glass Particles

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fresenius Kabi

FDA (recalls & safety alerts)

Consumer products

Reported Aug 11, 2026Updated Sep 17, 2026

Henkel Corp recalls Schwarzkopf Professional Extra Strong Mousse due to Due to Packaging Defect

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Henkel Corp.

FDA (recalls & safety alerts)

Reported Aug 9, 2026Updated Sep 17, 2026

Taylor Fresh Foods recalls Trader Joe’s, Freshness Guaranteed and more Finished products (e.g. dips, salsa, guacamole and more) containing jalapeno due to…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Taylor Fresh Foods

FDA (recalls & safety alerts)

Reported Aug 8, 2026Updated Sep 13, 2026

City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

City Foods, Inc./Bea's Best Corned Beef

USDA FSIS

Reported Aug 8, 2026

FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Reported Aug 7, 2026Updated Aug 25, 2026

Corte Argentino USA LLC Recalls Raw Beef Products Imported Without The Benefit Of Import Reinspection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Corte Argentino USA LLC

USDA FSIS

Reported Aug 7, 2026Updated Sep 17, 2026

Lexunder Inc. dba Food To Live recalls Food To Live Green Powder Products due to Possible Salmonella Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Lexunder Inc. dba Food To Live

FDA (recalls & safety alerts)

Reported Aug 7, 2026Updated Aug 25, 2026

Shan Distribution Network, Inc. Recalls Ineligible Frozen Siluriformes Breaded Fish Fillet and Stick Products Imported…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Shan Distribution Network, Inc.

USDA FSIS

Consumer products

Reported Aug 6, 2026

Liuqibax Adult Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Changsha 678 Trading Co., Ltd., dba Luqiba

CPSC

RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up