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. 2,648 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,648 in last 12 months

Showing 3118131200 of 55,896 recalls

Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Intuitive Surgical, Inc.

Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...

The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2017· MicroPort Orthopedics Inc.

Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...

The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...

The Issue: Increased amount of residual blood present on the top of stopper well after...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: Torque wrench used on the bolts for the Symbia T2 model 10275008 Recalled by...

The Issue: The torque wrench used to tighten system bolts during installation was found...

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

Class II — Potential Health HazardOngoing
FoodSeptember 18, 2017· Grand Supercenter Inc.

Recalled Item: HAIOREUM Recalled by Grand Supercenter Inc. Due to Undeclared Wheat

The Issue: The firm, Grand Supercenter Inc., was notified by USFDA NY District Office...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2017· Death Wish Coffee Company, LLC

Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...

The Issue: Potential for Clostridium Botulinum

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund