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. 2,683 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,683 in last 12 months

Showing 2230122320 of 29,496 recalls

Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension RxL Max HM STM Product Recalled by...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Flexible Screw Driver SJ706R Recalled by Aesculap, Inc. Due to The flexible...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· OrthoPediatrics Corp

Recalled Item: UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response...

The Issue: Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Zimmer, Inc.

Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Single...

The Issue: The firm identified a malfunction which made it possible for a handpiece to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Zimmer, Inc.

Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double...

The Issue: The firm identified a malfunction which made it possible for a handpiece to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2015· Medtronic Inc.

Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...

The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...

The Issue: The product may contain electronic components that lead to a premature...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2015· Vidco, Inc.

Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...

The Issue: Testing at customer site showed unit Remote Patient Monitoring System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Remel Inc

Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...

The Issue: Antibiotic concentration may be insufficient which may result in incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Myco Medical Supplies Inc

Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...

The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Terumo Medical Corporation

Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...

The Issue: Based on internal investigation and testing that revealed the distal end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2015· Brainlab AG

Recalled Item: RT Elements are applications for radiation treatment planning for use...

The Issue: Large objects with fine resolution are potentially displayed cropped when...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2015· Brainlab AG

Recalled Item: RT Elements are applications for radiation treatment planning for use...

The Issue: Large objects with fine resolution are potentially displayed cropped when...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2015· CareFusion 303, Inc.

Recalled Item: Alaris Pump SmartSite Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2015· Edwards Lifesciences, LLC

Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2015· Ormco/Sybronendo

Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...

The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing