Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,026 recalls have been distributed to New York in the last 12 months.

55,896 total recalls

2,026 in last 12 months

All Food Drug Medical Device Consumer Product Vehicle

Showing 16981–17000 of 55,896 recalls

Medical DeviceJuly 16, 2021· Teleflex Medical Europe Ltd

Recalled Item: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...

The Issue: The firm received reports that the endotracheal tube cuff could be inflated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 16, 2021· Teleflex Medical Europe Ltd

Recalled Item: RUSCH Endotracheal Tube oral/nasal Murphy Eye Recalled by Teleflex Medical...

The Issue: The firm received reports that the endotracheal tube cuff could be inflated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 16, 2021· Teleflex Medical Europe Ltd

Recalled Item: RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical...

The Issue: The firm received reports that the endotracheal tube cuff could be inflated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 16, 2021· Teleflex Medical Europe Ltd

Recalled Item: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...

The Issue: The firm received reports that the endotracheal tube cuff could be inflated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 15, 2021· Philips North America

Recalled Item: (1) Ingenia Ambition X (Product Number 781356) Recalled by Philips North...

The Issue: The sealed magnet will experience uncontrolled shutdown known as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 15, 2021· Beckman Coulter Inc.

Recalled Item: Normand Remisol Advance Data Manager Recalled by Beckman Coulter Inc. Due to...

The Issue: There is a potential that the data management system may add additional...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing

Medical DeviceJuly 15, 2021· Cell Marque Corporation

Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Mouse...

The Issue: Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing

DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF...

The Issue: cGMP Deviations