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. 2,492 recalls have been distributed to Maine in the last 12 months.
Showing 14741–14760 of 48,770 recalls
Recalled Item: Uncle Wally's Twin Muffins - Blueberry Recalled by GIVE AND GO PREPARED...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Chocolate Chip Snack Muffin - 12 oz Recalled by GIVE AND GO...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Worthy Crumb Assorted Large Muffins - Blueberry Streusel / Recalled by...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Banana Nut Snack Muffins - 12 oz. Recalled by GIVE AND GO...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Freshness Guaranteed Chocolate Chip Mini Muffins - 12 oz. Recalled by GIVE...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Wally's Twin Muffins - Banana Nut - 3.75oz Recalled by GIVE AND GO...
The Issue: May be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALPHA MALE+ Male Enhancer Recalled by Alpha-Tek LLC Due to Marketed Without...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Infant/Child...
The Issue: Infant/Child defibrillator pads contain incorrect labeling. This could lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Murphy Eye Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Ingenia Ambition X (Product Number 781356) Recalled by Philips North...
The Issue: The sealed magnet will experience uncontrolled shutdown known as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that the data management system may add additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Mouse...
The Issue: Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Beach Defense water + sun protection sunscreen spray BROAD...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.