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. 2,632 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,632 in last 12 months

Showing 3422134240 of 53,621 recalls

Medical DeviceNovember 8, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...

The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Meridian Bioscience Inc

Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...

The Issue: Internal testing has demonstrated that the indicated kit lots produce false...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
FoodNovember 8, 2016· Chaos and Pain

Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...

The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2016· Care-Tech Laboratories, Inc.

Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 7, 2016· Pfizer Inc.

Recalled Item: LEVOXYL(R) (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...

The Issue: Firm received reports about "acquisition errors" and the deterioration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Becton Dickinson & Company

Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...

The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Bayer Healthcare

Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...

The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Novation Cemented Plus Femoral Stem Recalled by Exactech, Inc. Due to...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Alteon Neck Preserving Stem Recalled by Exactech, Inc. Due to Products were...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...

The Issue: The device defect associated with this recall may result in HbA1c values...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Cincinnati Sub-Zero Products Inc

Recalled Item: The Hemotherm 400CE 115v Recalled by Cincinnati Sub-Zero Products Inc Due to...

The Issue: The device may not maintain water flow or temperature control.

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

Class II — Potential Health HazardOngoing