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. 1,781 recalls have been distributed to New Jersey in the last 12 months.
Showing 42981–43000 of 53,621 recalls
Recalled Item: EHMER COOKED ANDOUILLE SAUSAGE SEASONING (AND-119) 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.
Recalled Item: WORTHINGTON HOT SOUTHWESTERN SEASONING II- B Recalled by First Spice Mixing...
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.
Recalled Item: MYC Ingredients Recalled by Myc Ingredients Due to Undeclared Peanut
The Issue: Cumin may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PINATA'S ASADA SEASONING (SEA-164) Recalled by First Spice Mixing Co.,Inc....
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.
Recalled Item: SALSA PICA ASADA (SEA-268) Recalled by First Spice Mixing Co.,Inc. Due to...
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses...
The Issue: One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flyte Togas are components of the Stryker Flyte System and Recalled by...
The Issue: A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.