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 4684146860 of 53,621 recalls

DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2013· Good Neighbors Specialty Foods, LLC

Recalled Item: Good Neighbors Specialty Foods Tabouli Salad Recalled by Good Neighbors...

The Issue: Customer found blade inside the salad.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2013· Nutra Balance Products

Recalled Item: Thickened Water Nectar Thick 32 oz. (944ml) Phase 1 Ingredients: Recalled by...

The Issue: NUTRA Balance Thickened Water Nectar Thick was found by the FDA to contain...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2013· Nutra Balance Products

Recalled Item: Thickened Water Pudding Thick 32 oz. (944ml) Phase 3 Ingredients: Recalled...

The Issue: NUTRA Balance Pre-Thickened Water was found to contain mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· ITC-Nexus Dx

Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...

The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Spacelabs Healthcare, Llc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 18, 2013· Novartis Consumer Health

Recalled Item: Benefiber fiber supplement stick packs Recalled by Novartis Consumer Health...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: Possible break in the connector of the Force Sensor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Stryker Spine

Recalled Item: Specialty Straight Static Inserter Assembly Product Usage: This instrument...

The Issue: Stryker has received complaints from customers relating to fracture along...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing