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. 1,852 recalls have been distributed to New Jersey in the last 12 months.
Showing 40501–40520 of 53,621 recalls
Recalled Item: Papaverine/Phentolamine/Atropine/PGE-1 Injectable Recalled by Liberty Drug &...
The Issue: Lack of Assurance of Sterility: Process deficiencies were observed in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxocobalamin (Preserved) 10 Recalled by Liberty Drug & Surgical Due to...
The Issue: Lack of Assurance of Sterility: Process deficiencies were observed in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenol 6% Injectable Recalled by Liberty Drug & Surgical Due to Lack of...
The Issue: Lack of Assurance of Sterility: Process deficiencies were observed in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methadone 10 mg/mL Injection Recalled by Liberty Drug & Surgical Due to Lack...
The Issue: Lack of Assurance of Sterility: Process deficiencies were observed in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PYROLA Advanced Joint Formula capsules Recalled by GC Natural Nutrition,...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Precision RXi Digital system Recalled by GE Healthcare Due to...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1020 LipoTower with Aspiration Pump. Medical use. Recalled by MicroAire...
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE FB CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB PS ARTICULATION SURFACE SZ1-10 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...
The Issue: QC results were out of range resulting in false resistant strains.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...
The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...
The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP PS ARTICULATION SURFACE SZ1-9 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.