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. 2,776 recalls have been distributed to New York in the last 12 months.
Showing 14541–14560 of 30,153 recalls
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361 Recalled by Maquet...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-BEQ-TOP 33704 ECC 1/4" PACK Material: 701054150 Recalled by...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366 Recalled by...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287 Recalled by...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam...
The Issue: Weld attaching the air heater assembly to the main sterilizer unit has shown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...
The Issue: Incorrect raw material used by the supplier in the manufacturing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to A design...
The Issue: A design related issue can contribute to the device exhibiting brittle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.