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. 2,317 recalls have been distributed to Maine in the last 12 months.
Showing 38521–38540 of 48,770 recalls
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) Recalled by Arrow International Inc Due to Certain...
The Issue: Certain product codes and lot numbers of Kits with Biopatch Dressing were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...
The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...
The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...
The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walnut Pieces packaged in the following sizes and brand names: Recalled by...
The Issue: Product may be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due...
The Issue: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Epidural Needle Component (product number AN-05501). Epidural needles...
The Issue: The product labeling does not specify the 5 year shelf life of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPWorks software used in the Xltek Protektor Stimulator Product Usage:...
The Issue: Software error occurs when using remote monitoring; if the remote user tries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.