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 21161–21180 of 48,770 recalls
Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...
The Issue: Product may contain metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITAMIN B COMPLEX 100 (MDV) Recalled by RXQ Compounding LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 1MG/ML IN NACL 0.9% 55ML SYR (C-II) Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRAVASOL 10% (AMINO ACID) INJECTION SOLUTION Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUFFERED LIDOCAINE HCL 1% INJECTION SOL (PF) SYR Recalled by RXQ Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROMORPHONE 0.2MG/ML IN NACL 0.9% SYR (C-II) Recalled by RXQ Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ONDANSETRON 2 MG/ML INJECTION SOLUTION (PFV) Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.