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. 2,542 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,542 in last 12 months

Showing 52615280 of 27,655 recalls

Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Positioner Arm may not tighten or lock during normal use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· KENT IMAGING, INC.

Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...

The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· PHASE SCIENTIFIC INTERNATIONAL LIMITED

Recalled Item: INDICAID COVID-19 Rapid Antigen At-Home Test Recalled by PHASE SCIENTIFIC...

The Issue: COVID-19 rapid antigen at home tests were released with an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Becton, Dickinson and Company, BD Biosciences

Recalled Item: CD11b APC: ASR Recalled by Becton, Dickinson and Company, BD Biosciences Due...

The Issue: In vitro diagnostics product that impacts the quality of cell staining can...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Riverpoint Medical, LLC

Recalled Item: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) Recalled by...

The Issue: Use of a 1.4 drill in hard bone conditions caused increased insertion forces...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· GRAPHENANO DENTAL SL

Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...

The Issue: Machining error on cams renders the device unusable.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing