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. 2,642 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,642 in last 12 months

Showing 2804128060 of 53,621 recalls

Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE BLUE 18" 7-0 D/A BV-1 Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C Recalled by Ethicon, Inc....

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 36"(90CM) 3-0 BLU Recalled by Ethicon, Inc. Due to The needle...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 30"(75CM) 8-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PRONOVA SUTURE BLUE 122CM M1.5 Recalled by Ethicon, Inc. Due to The needle...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 4-36" (90CM) 3-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 36"(90CM) 4-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE MONO BLUE BV1755 Taperpoint 3/8C Recalled by Ethicon, Inc....

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 30"(75CM) 4-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...

The Issue: Potential for positively biased results

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Synthes (USA) Products LLC

Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...

The Issue: The adapter may demonstrate a degradation of function as the final products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Thermo Fisher

Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...

The Issue: Product may fail performance testing for S aureus ATCC 43300.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 43 Recalled by Beckman Coulter Inc. Due to...

The Issue: The drug dilution sequence for Moxifloxacin printed on the panel is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Vascular Solutions, Inc.

Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...

The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Stryker GmbH

Recalled Item: Farabeuf Clamp for 3.5mm Screws PRO Recalled by Stryker GmbH Due to Laser...

The Issue: Laser etching which indicates whether the device is in compression or...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.1 mg/day Recalled by Noven...

The Issue: Defective Delivery System: no longer meets the specification for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.0375 mg/day Recalled by Noven...

The Issue: Defective Delivery System: no longer meets the specification for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing