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. 2,603 recalls have been distributed to New Jersey in the last 12 months.
Showing 38861–38880 of 53,621 recalls
Recalled Item: Honey Mustard Pretzel Mix sold under the following brand and size: Girl...
The Issue: The honey mustard pretzel mix lists whey in the ingredient list but does not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marky's Puto Seko Special Recalled by Lee'S Food Corp Due to Undeclared Colors
The Issue: Lee Food Corporation is recalling Marky's Puto Seko Special because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Mustard Mix sold under the following brand: Ashdon Farms Recalled by...
The Issue: The honey mustard mix lists whey in the ingredient list but does not list...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Island Biscuit "Yum Yum - Creamy Strawberry" Biscuit Snack Recalled by Lee'S...
The Issue: Sampling analysis revealed the product contains undeclared colors (FD&C Red...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Butternut Squash Triangoli Recalled by Trader Joes Company Due to Undeclared...
The Issue: Trader Joe's is recalling Trader Giotto's Butternut Squash Triangoli because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DEXTROAMPHETAMINE SACCHARATE Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: High out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...
The Issue: An incorrect calibration of the thermometer that causes the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers:...
The Issue: During an internal testing, Natus Medical Incorporated, identified that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.