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. 1,777 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,777 in last 12 months

Showing 4870148720 of 53,621 recalls

FoodJuly 25, 2013· Thrive Foods LLC

Recalled Item: THRIVE 6 Grain Pancake Mix Recalled by Thrive Foods LLC Due to Thrive Foods...

The Issue: Thrive Foods is recalling certain lots of its 64 and 72 ounce cans of THRIVE...

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2013· Baxter Healthcare Corp.

Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...

The Issue: Defective Container: There is a potential for frangible components to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2013· Trumpf Medical Systems

Recalled Item: ORBIT PT. The ORBIT PT works in conjunction with an Recalled by Trumpf...

The Issue: An odor and smoke developed - The cause was determined to be a power supply...

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

Class III — Low RiskOngoing
Medical DeviceJuly 24, 2013· OrthoPediatrics Corp

Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...

The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Nestle HealthCare Nutrition

Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...

The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Gyrus Medical, Inc

Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...

The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2013· Microgenics Corp

Recalled Item: DRI Cocaine Metabolite Assay Recalled by Microgenics Corp Due to...

The Issue: Surveillance of reagent stability for specific lots of DRI Cocaine...

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Labeling -label error on declared strength: unopened, sealed bottle of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2013· Elekta, Inc.

Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...

The Issue: Potential for clinical errors.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Synthes USA HQ, Inc.

Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...

The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16-Slice CT Scanner System. Used as a whole-body computed Recalled by...

The Issue: A pinch point at the end of the table top can cause injury.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
FoodJuly 22, 2013· New Sun Inc

Recalled Item: New Sun JLB Combination Recalled by New Sun Inc Due to Potential E. coli...

The Issue: Positive E.coli

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 22, 2013· New Sun Inc

Recalled Item: New Sun Immune 101 Recalled by New Sun Inc Due to Potential E. coli...

The Issue: Positive E.coli

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2013· Torrent Pharma Inc

Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...

The Issue: Defective Container; This action is being taken as a precautionary measure...

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

Class II — Potential Health HazardOngoing
Refund