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. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 30301–30320 of 48,770 recalls
Recalled Item: Palmer's Candies Chocolate Pretzels with Frosted Swirl NET WT 28 lbs (12.7...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Palmer's Candies Chocolatey Pretzels NET WT 28 lbs (12.7 kg) Recalled by...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Palmer's Candies Chocolatey Flavored NP Heart Pretzels NET WT 28 lbs (12.7...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Holiday White Peppermint Hostess Twinkies Recalled by Hostess Brands, LLC...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Generators may have a faulty component which could impact the proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) has identified that in a rare sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast sodium tablets Recalled by Hetero USA Inc Due to Discoloration:...
The Issue: Discoloration: the firm received a complaint of a sealed bottle in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...
The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...
The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System - C-Spine Coil Recalled by Hitachi Medical Systems...
The Issue: The customer indicated that the coil balun was hot to the touch when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...
The Issue: There is a possibility for data to be stored under the wrong patient on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: The company received a customer complaint for the inability to calibrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cappuccino Snack Mix Lot code: 20161027 Recalled by Dutch Valley Food...
The Issue: As a result of an ingredient supplier recall, Dutch Valley is issuing a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.