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. 2,696 recalls have been distributed to New Jersey in the last 12 months.
Showing 19821–19840 of 29,496 recalls
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.
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.
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.
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.
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.
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.
Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...
The Issue: Due to a customer experiencing complaints on bone fraction of assay not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...
The Issue: The firm failed to notify current customers of IFU update/warning. During a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue where certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...
The Issue: Software malfunction that results in incorrect generation or display of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...
The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adiprep Adipose Transfer System. Product Codes: 51431 Recalled by Terumo...
The Issue: Terumo BCT announces a voluntary field action for the Harvest : Adiprep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
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: Siemens is releasing a software update that provides bug-fixes to improve...
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: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...
The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...
The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.