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. 2,748 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,748 in last 12 months

Showing 1646116480 of 55,896 recalls

Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2021· North Coast Medical Inc

Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2021· PTW NORTH AMERICA CORPORATION

Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...

The Issue: When a measurement with a PTW detector array is performed with the software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2021· North Coast Medical Inc

Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2021· Uoc Usa Inc

Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...

The Issue: Due to product not meeting specification for concentricity and failing to...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF Recalled by DuPont...

The Issue: Microbial Contamination of Non-Sterile Product: Out-of-specification results...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fulvestrant Injection 250 mg/5 mL (50 mg/mL) For Intramuscular Use Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund