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. 2,567 recalls have been distributed to New York in the last 12 months.
Showing 45841–45860 of 55,896 recalls
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.
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.
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.
Recalled Item: 8MM FENESTRATED BIPOLAR FORCEPS 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.
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.
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.
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.
Recalled Item: 8MM PERMANENT CAUTERY SPATULA 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.
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.
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.
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.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...
The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
Recalled Item: Mt. Olive Recalled by Mt. Olive Pickle Company Inc Due to Product may...
The Issue: Product may contain glass fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.