infant product Recalls

794 recalls tagged with “infant product”.

Vehicles & Parts
HIGH
NHTSA

AUDI SQ7 Recalled for Fuel Pump Fastener Tightening Issue in 2025 Model

Volkswagen Group of America recalls one 2025 Audi SQ7 over a potential fuel leak from an improperly tightened high pressure fuel pump. The recall affects a single vehicle and is classified as high risk due to fire potential. Owners should contact Volkswagen for inspection and repair at no cost.

AUDI
A fuel
Read more
Food & Beverages
HIGH
FDA FOOD

Orwashers Soho Sourdough XL Batard Recalled for Undeclared Sesame Seeds

Orwashers brand Soho Sourdough XL Batard is being recalled after labeling errors could hide sesame seeds. The recall covers 4 pallets of 6 pieces per case in Massachusetts. Consumers should avoid consumption and contact Oven Artisans LLC for refunds or replacements.

Orwashers
Mislabeled: Product
Read more
Health & Personal Care
HIGH
FDA DRUG

Zydus Entacavir Recall 600 Bottles Over Impurity Degradation Issue (2025)

Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.

Entacavir
Failed impurity/degradation
Read more
Food & Beverages
HIGH
FDA FOOD

Southwind Foods' Tovala-brand Frozen Shrimp Recalled for Cs-137 Contamination (93,122 Cases, 2025)

Southwind Foods LLC, doing business as Great American Seafood Imports, recalled 93,122 cases of Tovala-brand frozen raw phosphate-free shrimp after identifying potential Cesium-137 contamination. The recall expands a prior action and notes insanitary production conditions. Consumers who bought the 5 oz IQF bag with UPC 829944085788 should not eat it and should contact the supplier for refund or re

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
Read more
Health & Personal Care
HIGH
FDA DEVICE

BD EpiCenter Recall: 2,050 Units Worldwide Over Unauthorized Access Risk

BD recalled 2,050 units of the EpiCenter Microbiology Data Management System due to unauthorized access to product service credentials. The defect could allow access to confidential data. Stop using affected devices and follow manufacturer guidance for updates or replacement.

Becton Dickinson &
Product service
Read more
Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Free Range Grade AA Eggs Recalled for Salmonella Risk (20,625 Dozen) 2025

Black Sheep Egg Company recalled 20,625 dozen eggs sold at retail and wholesale locations in Arkansas and Missouri after a potential Salmonella contamination. The eggs are Free Range Grade AA Large Brown, loose-packed in boxes. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
Read more
Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 58,500 Dozen Free Range Eggs for Salmonella Risk (2025)

Black Sheep Egg Company recalls 58,500 dozen free range Grade AA medium brown eggs after FDA enforcement notice citing potential Salmonella contamination. The recall covers eggs sold in Arkansas and Missouri, with wholesale and broker locations in Mississippi, Texas, California and Indiana. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refund or replacement.

Black Sheep Egg Company
Potential Salmonella
Read more
Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 16,245 Dozen Free Range Eggs (18ct) 2025

Black Sheep Egg Company recalled 16,245 dozen Free Range Grade A Large Brown Eggs sold at retail locations in Arkansas and Missouri, and through wholesale brokers in Mississippi, Texas, California and Indiana. The cartons carry UPC 860010568538. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
Read more
Health & Personal Care
HIGH
FDA DEVICE

Kico Knee Innovation ARVIS Shoulder AI Planning Software Recalled for High-Risk Malalignment in 21-0

Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.

Kico Knee Innovation
Complaint identified
Read more
Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale locations in Arkansas and Missouri. The recall centers on potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement information.

Black Sheep Egg Company
Potential Salmonella
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.

Beckman Coulter
Beckman Coulter
Read more