Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,653 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,653 in last 12 months

Showing 2480124820 of 29,496 recalls

Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...

The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...

The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2014· Advandx Inc

Recalled Item: AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures) Recalled by Advandx...

The Issue: Positive result in the Internal negative control well for the Staphylococcus...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/...

The Issue: Unsealed pouches.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Intelerad Medical Systems

Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...

The Issue: In specific situation a partially truncated file may be written to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with Unitized Catheter and Accessories...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Mentor Texas, LP.

Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...

The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing