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. 2,564 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,564 in last 12 months

Showing 4298143000 of 53,621 recalls

FoodDecember 24, 2014· First Spice Mixing Co.,Inc.

Recalled Item: TACO PERFECTOS ALL-PURPOSE SEASONING (SEA-323) Recalled by First Spice...

The Issue: Firm was notified by immediate supplier that certain lots of ground cumin...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 24, 2014· First Spice Mixing Co.,Inc.

Recalled Item: RIEKER GRILL & BRATEN (SAU-048) Recalled by First Spice Mixing Co.,Inc. Due...

The Issue: Firm was notified by immediate supplier that certain lots of ground cumin...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 24, 2014· N.A.C. Foods

Recalled Item: Rosa Maria Ground Cumin Recalled by N.A.C. Foods Due to Undeclared Peanut

The Issue: N.A.C. Foods initiated this recall because Mimi's Products Ground Cumin and...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 24, 2014· Schiff Foods Products

Recalled Item: Ground Cumin Seeds Recalled by Schiff Foods Products Due to Cumin may be...

The Issue: Cumin may be contaminated with peanut protein.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 24, 2014· N.A.C. Foods

Recalled Item: Mimi's Products Ground Cumin Recalled by N.A.C. Foods Due to Undeclared Peanut

The Issue: N.A.C. Foods initiated this recall because Mimi's Products Ground Cumin and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2014· Baxter Healthcare Corp.

Recalled Item: Fluconazole Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints of leaks due to an incomplete...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2014· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: The firm received a complaint of an embedded...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 23, 2014· Hi-Tech Pharmacal Co., Inc.

Recalled Item: FERROUS SULFATE ELIXIR 220 mg/5 mL Recalled by Hi-Tech Pharmacal Co., Inc....

The Issue: Out-of-specification result for pH observed during stability testing of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx monitor/defibrillator Models M3535A Recalled by Philips...

The Issue: MRx monitor/defibrillator could reboot at an indeterminate time, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2014· Therasage, LLC.

Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...

The Issue: Product distributed without 510(k) approval

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2014· Therasage, LLC.

Recalled Item: Portable FAR Infrared Sauna Indications including Recalled by Therasage,...

The Issue: Product distributed without 510(k) approval

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2014· Therasage, LLC.

Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...

The Issue: Product distributed without 510(k) approval

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2014· Shape Medical Systems, Inc

Recalled Item: Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI)....

The Issue: This recall has been initiated because use of the impacted DPIs could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2014· Cardinal Health

Recalled Item: Lubricated Intubating Stylet 6FR that is inserted into an endotracheal...

The Issue: A small piece of the stylet sheath has the potential to shear off upon...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2014· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product has the potential for solution...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2014· Qualitest Pharmaceuticals

Recalled Item: ACETAMINOPHEN and CODEINE PHOSPHATE ORAL SOLUTION USP Recalled by Qualitest...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
FoodDecember 22, 2014· Bidart Bros.

Recalled Item: Gala Apples "Big B" Recalled by Bidart Bros. Due to Recall of Granny Smith...

The Issue: Recall of Granny Smith Apples from 2014 harvest used in caramel apple...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 22, 2014· Bidart Bros.

Recalled Item: Granny Smith Apples Recalled by Bidart Bros. Due to Recall of Granny Smith...

The Issue: Recall of Granny Smith Apples from 2014 harvest used in caramel apple...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 22, 2014· Full Tilt Ice Cream

Recalled Item: Port Townsend Lavender ice cream Recalled by Full Tilt Ice Cream Due to...

The Issue: Full Tilt Brand ice cream is being recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund