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. 2,549 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,549 in last 12 months

Showing 4792147940 of 53,621 recalls

Medical DeviceSeptember 24, 2013· Beckman Coulter Inc.

Recalled Item: COULTER LH 750 and LH 780 Analyzers. The COULTER LH Recalled by Beckman...

The Issue: The check valves may fail on the Coulter LH 750 Hematology Analyzer (PN...

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

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2013· Tolmar, Inc.

Recalled Item: Ketoconazole Shampoo Recalled by Tolmar, Inc. Due to Subpotent

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· Watson Laboratories Inc

Recalled Item: Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet)...

The Issue: Failed Tablet/Capsule Specifications: Multiple complaints for push through...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Ivoclar Vivadent, Inc.

Recalled Item: ExciTE F DSC Soft touch Single Dose Recalled by Ivoclar Vivadent, Inc. Due...

The Issue: Ivoclar Vivadent, Inc. is recalling a lot of ExciTE F DSC Dental Adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Baylis Medical Corp *

Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...

The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs  25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Regional Anesthesia Tray with Drugs Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Alere San Diego, Inc.

Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...

The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...

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

Class III — Low RiskOngoing