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. 2,622 recalls have been distributed to New Jersey in the last 12 months.
Showing 35501–35520 of 53,621 recalls
Recalled Item: JUST Devil's Food Cake Mix Recalled by Hampton Creek Foods Due to Potential...
The Issue: Firm received a positive test result for Salmonella in Coconut Milk powder...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co....
The Issue: Ground Turmeric may contain excess levels of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: C-PAV/PHENTOL/PGE1 Recalled by Colonia Care Pharmacy Due to Lack of...
The Issue: Lack of Assurance of Sterility; sterility concerns with all injectable drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C-PAV/PHENTOL/ATROP/PGE1 Recalled by Colonia Care Pharmacy Due to Lack of...
The Issue: Lack of Assurance of Sterility; sterility concerns with all injectable drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hospira MedNet Medication Management Suite software Recalled by Hospira...
The Issue: Hospira MedNet 6.1 software, in combination with the SapphirePlus 13.1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE VC150 Vital Signs Monitor Recalled by INNOKAS MEDICAL OY Due to A...
The Issue: A software error on released software versions 1.6.12, 1.6.12F and 1.6.16...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SODIUM BICARBONATE Recalled by Natrium Products Inc Due to Sodium...
The Issue: Sodium Bicarbonate bulk lot 08315A may contain varying amounts of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: product was out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...
The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...
The Issue: If an affected Patient Monitor has been powered on continuously for several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz Recalled by La...
The Issue: Calcium caseinate is declared on the label, but milk is not listed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Slow Roasted Ham & Swiss Breakfast Sandwich Recalled by SK Food Group...
The Issue: The product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.