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. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 23981–24000 of 55,896 recalls
Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System Tubing Set kits Product numbers:...
The Issue: The firm received complaints on the saline tubing of Visualase Cooled Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...
The Issue: The firm updated the IFU in April 2019 to clarify that use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapsoCam Plus *** System Recalled by Capso Vision, Inc. Due to Possible...
The Issue: Possible mis-labeling of the device with incorrect serial number labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaLift Access Device Recalled by PediaLift LLC Due to The firm was...
The Issue: The firm was unsuccessful in obtaining a satisfactory Certificate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The Recalled by...
The Issue: Perfusion tubing pack was packaged with the incorrect cuvette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...
The Issue: Error in the default configuration which could lead to the incorrect display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.