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. 2,658 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,658 in last 12 months

Showing 2348123500 of 29,496 recalls

Medical DeviceApril 9, 2015· BTE Technologies, Inc.

Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...

The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Synthes, Inc.

Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...

The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Spinal Elements, Inc

Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...

The Issue: Some rods may not meet the appropriate traceability requirements including...

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

Class III — Low RiskOngoing
Medical DeviceApril 9, 2015· Bard Peripheral Vascular Inc

Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...

The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Coloplast Manufacturing US, LLC

Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...

The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2015· Baxter Corporation Englewood

Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...

The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2015· X Spine Systems Inc

Recalled Item: Fortex" Pedicle Screw System Continuous Radius Rod 5.5 - 50mm Recalled by X...

The Issue: The Continuous Radius Rod should measure 50mm in length but actually...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· GA Industries

Recalled Item: Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces...

The Issue: GA Industries is recalling the Logicon Caries Detector, version 5.0, for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: Assay Data Disk (ADD) Recalled by Ortho-Clinical Diagnostics Due to Software...

The Issue: Software anomaly regarding urine samples that require acidified...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly...

The Issue: Software anomaly regarding urine samples that require acidified...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2015· Carefusion 211 Inc dba Carefusion

Recalled Item: CareFusion AVEA ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: A pressure transducer failure can develop, activating a false Extended High...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 3, 2015· Medtest Holdings, Inc.

Recalled Item: Liquid stable 2 part Homocysteine Reagent Recalled by Medtest Holdings, Inc....

The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· MELA Sciences, Inc.

Recalled Item: MelaFind Device Recalled by MELA Sciences, Inc. Due to The probability and...

The Issue: The probability and histogram data within the Melafind's device displayed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Elite Care Cliner w/Swing Away Arms X-Large - with Nylon Casters...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Drop Arm Care Cliner X-Large - with Nylon Casters Oncology Recalled by...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Recalled...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Care Cliner X-Large - with Nylon Casters Oncology Recalled by Winco...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Nocturnal Elite Care Cliner - with Nylon Casters Lay Recalled by Winco...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing