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. 2,703 recalls have been distributed to New York in the last 12 months.
Showing 21041–21060 of 30,153 recalls
Recalled Item: T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch Recalled by...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker AutoPlex System. Model Numbers 0607-687-000 Recalled by Stryker...
The Issue: The Piston Head can become separated from the Delivery Piston, blocking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-000WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T090-000V 90" 20 Drop IV Admin Set w/ Needlefree Y-Site. Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...
The Issue: The pouch label was missing the use by date (UBD) of 2018-04.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard Allan Scientific 10% Neutral Buffered Formalin Recalled by...
The Issue: potential contamination with potassium hydroxide may have an impact when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic has...
The Issue: Medtronic has voluntarily decided to retrieve unused Model 3387S-40 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSP Hip Fracture Plating System device Recalled by Biomet, Inc. Due to...
The Issue: The screw may fracture at the junction of the shaft and the head during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dako HER2 CISH pharmDx Kit Recalled by Dako North America Inc. Due to An...
The Issue: An incorrect HER2 probe concentration was used when producing the probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...
The Issue: There is a potential for stylet stiffening that is not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...
The Issue: There is a potential for stylet stiffening that is not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preamendments device-Sarns Dual Cooler-Heater. The Sarns Dual Cooler-Heater...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HX2" Temperature Management Systems Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System Controller Product Usage: For use as...
The Issue: Loose connector ports in controller body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMD-Ritmed Transparent Dressing - Window with label Recalled by Amd-Ritmed,...
The Issue: The lot of transparent dressing was found to be contaminated (not sterile)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.