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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 25001–25020 of 48,770 recalls
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...
The Issue: Microbial Contamination of Sterile Products: Product associated with reports...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...
The Issue: Subpotent Drug and Failed Content Uniformity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Classic Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.