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. 2,771 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,771 in last 12 months

Showing 1564115660 of 30,153 recalls

Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare HEATWRAPS JOINT PAIN THERAPY Recalled by Pfizer Inc. Due to The...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 10x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 Deg 10x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Straumann Manufacturing, Inc.

Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...

The Issue: Laser engraved label does not match with the item in the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Randox Laboratories Ltd.

Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Randox Laboratories Ltd.

Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· SVS LLC

Recalled Item: PremierPro Aluminum Adjustable Walker Recalled by SVS LLC Due to This recall...

The Issue: This recall is due to a mandated order from the FDA for stock recovery and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Paragon 28, Inc.

Recalled Item: P28 Recalled by Paragon 28, Inc. Due to Mislabeling

The Issue: It has been determined that the wedge implant kit is permanently mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...

The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing