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. 2,812 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,812 in last 12 months

Showing 1306113080 of 30,153 recalls

Medical DeviceDecember 16, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...

The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Nextremity Solutions

Recalled Item: Stratum Lapidus Plate - Small Rt Recalled by Nextremity Solutions Due to The...

The Issue: The product contains a different plate than indicated by the package...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...

The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Clinical Chemistry Control Recalled by Randox Laboratories Ltd. Due...

The Issue: A transcription error has occurred for the Randox Lipase colorimetric value...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 13, 2019· CooperSurgical, Inc.

Recalled Item: ADVANCED ENDOSEE System CANNULA Recalled by CooperSurgical, Inc. Due to...

The Issue: Potential for unsealed pouches in two (2) lots of the Endosee Advance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: Clearlink System Continu-Flo Administration Sets Recalled by Baxter...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: ONE-LINK Needle-free IV Connector Recalled by Baxter Healthcare Corporation...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Health Network Strips- intended for Blood Glucose...

The Issue: Inability to dose the test strips, may result in a temporary inability to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- Umbilical Trays UVT1045 UMBILICAL ARTERY TRAY UVT1055 UVC KIT...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing