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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 21861–21880 of 48,770 recalls
Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer Recalled by Inopak Ltd Due to...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ANTIBACTERIAL Foaming Hand Wash With Moisturizers labeled as Antibacterial...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQUACIL instant foaming hand sanitizer Recalled by Inopak Ltd Due to CGMP...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FENTANYL Transdermal System Recalled by Alvogen, Inc Due to Product Mix-Up:...
The Issue: Product Mix-Up: Customer complaint that their carton labeled as Fentanyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This...
The Issue: Defective Delivery System: difficult to express
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...
The Issue: Images may potentially become corrupt while using the system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...
The Issue: Reports of aspirating biopsy needle breakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.