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. 999 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
999 in last 12 months

Showing 45841–45860 of 55,896 recalls

Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM MONOPOLAR CURVED SCISSORS Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
FoodNovember 3, 2014· Raymond-Hadley Corp.

Recalled Item: Pride of Africa brand Semo "Semolina" Recalled by Raymond-Hadley Corp. Due...

The Issue: Label review revealed the product contains undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 3, 2014· Raymond-Hadley Corp.

Recalled Item: Pride of Africa brand Farina Recalled by Raymond-Hadley Corp. Due to...

The Issue: Label review revealed the product contains undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 3, 2014· House Of Spices (india) Inc.

Recalled Item: LAXMI NUTKHHAT Golden Raisins Recalled by House Of Spices (india) Inc. Due...

The Issue: The product contained undeclared sulfites based on sampling and analysis by...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 31, 2014· Nature's Way Purewater Systems, Inc.

Recalled Item: ESSENTIA Hydration Perfected Purified Water and Electrolytes Recalled by...

The Issue: Product may contain mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2014· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...

The Issue: Software upgrade to correct potential safety issue related to CyberKnife...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2014· Alcon Research, Ltd.

Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....

The Issue: Alcon is conducting a medical device recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2014· Carestream Health, Inc.

Recalled Item: CARESTREAM DIRECTVIEW CR Software Generates digital mammographic images that...

The Issue: Reduced mammographic image quality when attempting to print true size...

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

Class II — Potential Health HazardOngoing
DrugOctober 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug: Heparin raw material was found to have low potency

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2014· Respironics California Inc

Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...

The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2014· Remel Inc

Recalled Item: Remel TB Potassium Permanganate (.5% Aqueous) 40192 Recalled by Remel Inc...

The Issue: The product may appear cloudy or discolored and may not perform correctly in...

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

Class II — Potential Health HazardOngoing