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. 2,536 recalls have been distributed to Maine in the last 12 months.
Showing 5861–5880 of 27,655 recalls
Recalled Item: ProPlan CMF Patient-Specific Guide Recalled by Materialise N.V. Due to Wrong...
The Issue: Wrong versions of guides 3A and 3B (Patient Specific) were shipped prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONFORMIS HIP-SCREW-6.5MM X 25MM Recalled by Conformis, Inc. Due to 30mm...
The Issue: 30mm screws were labeled as 25mm screws.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Infant Heel Warmer Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health has received an increase in burst/leaking complaints from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOLOMITE GLOSS ROLLATOR - intended to support during walking and Recalled by...
The Issue: Premature failure of the seat during use, the plastic eyelets of the folding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: 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.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
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: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.