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. 2,861 recalls have been distributed to New York in the last 12 months.
Showing 5501–5520 of 30,153 recalls
Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCF-H190L Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIF-H190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may have...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIF-HQ190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits:...
The Issue: Produced with unintended open slits on the side of the mouthpiece body, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-i Recalled by Maquet Medical Systems USA Due to It was found that...
The Issue: It was found that the fixation (weld) employed by the supplier of the nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-XT190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150 Recalled by Olympus...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T180...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190 Recalled by Olympus...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number Q180-AC...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.