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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 8361–8380 of 48,770 recalls
Recalled Item: MEGADYNE Suction Coagulators Recalled by Megadyne Medical Products, Inc. Due...
The Issue: An issue with the Suction Coagulator product family may lead to fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella LD intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.0 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist intravascular micro axial blood pump Recalled...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP with SmartAssist intravascular micro axial blood pump Recalled by...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Direct Amplification Disc Kit Recalled by DiaSorin Molecular LLC...
The Issue: There is a potential for the direct amplification disc to malfunction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 2.5 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Eye Relief Lubricant Eye Drops Recalled by K.C. Pharmaceuticals, Inc Due...
The Issue: CGMP Deviations: good manufacturing deficiencies related to a lack of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Original Eye Drops Recalled by K.C. Pharmaceuticals, Inc Due to CGMP...
The Issue: CGMP Deviations: good manufacturing deficiencies related to a lack of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranexamic Acid USP Tablets Recalled by AVKARE LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) Recalled by...
The Issue: Carryover from the Direct LDL-cholesterol assay on the Rx instruments may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2 Recalled...
The Issue: Dura regeneration matrix may have out-of-specification endotoxin levels due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrin (progesterone) Vaginal Insert 100mg Recalled by Ferring...
The Issue: cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lysteda (tranexamic acid) USP Tablets Recalled by Amring Pharmaceuticals Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Havasu Beetroot Powder Recalled by Supplement Manufacturing Partner, Inc....
The Issue: Contains undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.