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 20781–20800 of 30,153 recalls
Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...
The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...
The Issue: If an affected Patient Monitor has been powered on continuously for several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite F50 instrument. The INFINITE F50 instrument is a 96-well Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNRISE instrument. The INFINITE F50 instrument is a 96-well absorbance...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...
The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...
The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroflex ELISA The HYDROFLEX is a plate washer for 96-well Recalled by...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite M1000 PRO The Tecan Infinite M1000 PRO is Recalled by Tecan...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite 200. The SUNRISE instrument is a 96-well absorbance Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO The Tecan Infinite 200 PRO is a Recalled by Tecan US, Inc....
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...
The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.