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. 2,551 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,551 in last 12 months

Showing 4582145840 of 53,621 recalls

Medical DeviceApril 29, 2014· Synthes, Inc.

Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...

The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Connection issues between the PD transfer set catheter connector and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal Chest Drain ATS Blood Recovery Recalled by Atrium...

The Issue: Product that was previously recalled because the Chest Drain tubing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Greatbatch Medical

Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...

The Issue: Greatbatch identified that the documentation does not support the five-year...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
FoodApril 25, 2014· American Licorice Company

Recalled Item: REDVINES FRUIT VINES Bites Cherry ARTIFICIALLY FLAVORED NET WT Recalled by...

The Issue: The nutritional panel on the packaging incorrectly states the sodium content...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodApril 25, 2014· American Licorice Company

Recalled Item: REDVINES FRUIT VINES Bites Strawberry ARTIFICIALLY FLAVORED NET WT Recalled...

The Issue: The nutritional panel on the packaging incorrectly states the sodium content...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 25, 2014· Hitachi Medical Systems America Inc

Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...

The Issue: The firm received a complaint stating the Coil Extension Cable accessory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...

The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· CryoLife, Inc.

Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...

The Issue: Serum albumin component monomer failed to meet internally established end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoBaby Vanilla Organic Whole Milk Yogurt multipack 6 pack...

The Issue: Product has elevated levels of coliforms

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoToddler Raspberry/Pear Cereal Organic Whole Milk Yogurt with...

The Issue: Product has elevated levels of coliforms

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoBaby Pear/Peach Organic Whole Milk Yogurt multipack- 6 pack...

The Issue: Product has elevated levels of coliforms

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...

The Issue: System error 01779 is produced when the battery cannot be charged due to...

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

Class II — Potential Health HazardOngoing