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. 2,816 recalls have been distributed to New Jersey in the last 12 months.
Showing 10381–10400 of 53,621 recalls
Recalled Item: Simvastatin Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropinirole Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropinirole Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Montelukast Sodium Tablets Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Recalled by Direct Rx Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Perrona Hot Sauce Original with Chiltepin Peppers 5 fl oz Recalled by...
The Issue: Mold growth on the outside of the bottle
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL Recalled by TIPPCON...
The Issue: Mold growth on the outside of the bottle
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perrona Hot Sauce Green with Chiltepin Peppers Net 5 FL Recalled by TIPPCON...
The Issue: Mold growth on the outside of the bottle
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Quantum Perfusion Systems for CPB Recalled by Spectrum Medical Ltd. Due to...
The Issue: The ratchet and pawl had an out of tolerance geometry which exhibited as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.