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. 1,781 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,781 in last 12 months

Showing 4328143300 of 53,621 recalls

DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaints received for...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Product is subpotent and has out of...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Leonhard Lang Gmbh

Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...

The Issue: The firm discovered that during the use of these defibrillation electrodes a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Ferno-Washington Inc

Recalled Item: Ferno Model 35X PROFlexx Stretchers Recalled by Ferno-Washington Inc Due to...

The Issue: The wheel castor assemblies may be loosening on the stretchers.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...

The Issue: Suboptimal routing of the cable may result in increased wear over time....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUX Material Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUX Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing