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. 2,549 recalls have been distributed to New Jersey in the last 12 months.
Showing 53281–53300 of 53,621 recalls
Recalled Item: McClure's Pies & Salads Recalled by McClures, Inc. Due to Undeclared Allergens
The Issue: Undeclared allergens. Ingredient statement lists "flour" but is not specific...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: McClure's Pies & Salads Recalled by McClures, Inc. Due to Undeclared Allergens
The Issue: Undeclared allergens. Ingredient statement lists "flour" but is not specific...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: McClure's Pies & Salads Recalled by McClures, Inc. Due to Undeclared Allergens
The Issue: Undeclared allergens. Ingredient statement lists "flour" but is not specific...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: McClure's Pies & Salads Recalled by McClures, Inc. Due to Undeclared Allergens
The Issue: Undeclared allergens. Ingredient statement lists "flour" but is not specific...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunquest Laboratory : intended for use by professionals working in Recalled...
The Issue: Online calculations may not be performed as expected or may yield results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic retrieval device. The disposable Raptor grasping device in...
The Issue: When the outer catheter is either coiled or in a contorted configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep with Tint Recalled by Carefusion 213, Llc Due to Lack of...
The Issue: Lack of Assurance of Sterility: A customer complaint reported some units had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Implant Recalled by Biomet 3i, LLC Due to On November 3, 2011 Biomet 3i,...
The Issue: On November 3, 2011 Biomet 3i, Palm Beach Gardens, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory Recalled by Sunquest Information Systems, Inc. Due to...
The Issue: Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion Workstation. Recalled by Merge Healthcare, Inc. Due to After a period...
The Issue: After a period of time running Fusion Workstation, the Hounsfield...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7U163CS-36 In combination with below systems MUX-100H Recalled by Shimadzu...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.4/0.7JG326D-265AX/AT Product Usage: The device is a mobile X-ray system...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-20J Recalled by Shimadzu Medical Systems Due to Shimadzu is recalling...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-30H Recalled by Shimadzu Medical Systems Due to Shimadzu is recalling...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...
The Issue: The tip of the product could come loose or unravel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to As part of GE Innova IQ...
The Issue: As part of GE Innova IQ table introduction, a label was designed to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a Recalled by...
The Issue: Linear performance information in product insert does not match that listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software Product Usage: CADstream is an image processing system...
The Issue: Customers may experience an issue with the software study preferences when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.