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. 2,546 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,546 in last 12 months

Showing 38613880 of 27,655 recalls

Medical DeviceMay 10, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...

The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Stryker GmbH

Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...

The Issue: The adjustment ring on the device may become loose resulting in the wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· C.R. Bard Inc

Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...

The Issue: Some of the devices may function incorrectly resulting in no temperature...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...

The Issue: Simultaneous ECG measurements with multiple devices, including a manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2024· Baxter Healthcare Corporation

Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...

The Issue: There is a potential for the top cover of the hospital bed mattress to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...

The Issue: System monitor screen may display atypical behavior: Overlapping...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2024· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...

The Issue: Reports of patient burns.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...

The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...

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

Class III — Low RiskOngoing
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Impact Recalled by MEDLINE...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing