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. 2,715 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,715 in last 12 months

Showing 1698117000 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 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
DrugJuly 16, 2021· Alpha-Tek LLC

Recalled Item: ALPHA MALE+ Male Enhancer Recalled by Alpha-Tek LLC Due to Marketed Without...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
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· 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
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 14, 2021· Pentax of America Inc

Recalled Item: Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models:...

The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2021· Pentax of America Inc

Recalled Item: Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One...

The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2021· Ostial Corporation

Recalled Item: FLASH Ostial System Recalled by Ostial Corporation Due to Angioplasty system...

The Issue: Angioplasty system has a manufacturing issue that has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2021· Smith & Nephew Orthopaedics Ltd. (Aurora)

Recalled Item: smith&nephew BHR SQUARE HEADED NAIL Recalled by Smith & Nephew Orthopaedics...

The Issue: The nail head may become detached during surgery.

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

Class II — Potential Health HazardOngoing
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Aveeno Protect + sunscreen weightless spray with oat SPF 60 Recalled by...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50 Recalled by...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...

The Issue: Chemical Contamination: presence of benzene

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 70 Recalled by...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 100 Recalled by...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY Broad Spectrum SPF...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Beach Defense water + sun protection sunscreen spray BROAD...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund