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. 1,053 recalls have been distributed to New York in the last 12 months.
Showing 34101–34120 of 55,896 recalls
Recalled Item: PRK Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Operation Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Basic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes Recalled...
The Issue: BD is initiating this product correction of multiple lots of BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Wischmeier Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIVERSAL FLEX2 BREATHING CIRCUIT Recalled by King Systems Corp. dba Ambu,...
The Issue: Potential for leak test failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.