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. 2,499 recalls have been distributed to Maine in the last 12 months.
Showing 13221–13240 of 48,770 recalls
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amy's Vegan Organic Rice Mac & Cheese Recalled by Amys Kitchen Inc Due to...
The Issue: Firm investigation detected trace amounts of milk through finished product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The clip store function in the ultrasound imaging system does not work when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...
The Issue: Failed Dissolution Specification: Dissolution results are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...
The Issue: Devices may lose functionality due to susceptibility to moisture ingress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...
The Issue: individual components have been labelled with incorrect colours. The red and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Collagen Plugs Recalled by Lacrimedics Inc Due to The sterile pouch seal may...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPAQUE Herrick Lacrimal Plugs Recalled by Lacrimedics Inc Due to The sterile...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution Recalled by Aurobindo Pharma USA Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lexette (halobetasol propionate) Topical Foam Recalled by Mayne Pharma Inc...
The Issue: CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)Traverse Rail Carrier E-System Recalled by Hill-Rom, Inc. Due to Traverse...
The Issue: Traverse rail carriage delivered with non-conforming screws are too short to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1688 Camera Control Unit (CCU) Recalled by Stryker Corporation Due to A...
The Issue: A software defect in the camera control unit (CCU) will cause the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRRUS HD-OCT Recalled by Carl Zeiss Meditec, Inc. Due to Optic nerve head...
The Issue: Optic nerve head angiography scan to be turned off due to its distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.