Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 9541–9560 of 48,770 recalls
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.
Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JARDIANCE (Empagliflozin) Recalled by Boehringer Ingelheim Pharmaceuticals,...
The Issue: Labeling: Label Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.