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. 2,379 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,379 in last 12 months

Showing 2372123740 of 48,770 recalls

Medical DeviceAugust 28, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...

The Issue: There is a potential to generate falsely elevated serum or plasma chloride...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...

The Issue: The reagent pack exhibits the potential for an increased frequency of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...

The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due...

The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2018· QuVa Pharma, Inc.

Recalled Item: Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 Recalled by QuVa...

The Issue: Subpotent Drug: Product may not have the active ingredient present in the bag.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 27, 2018· Arthrex, Inc.

Recalled Item: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product...

The Issue: The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not...

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2018· LGM Pharma LLC

Recalled Item: Thyroid Powder Recalled by LGM Pharma LLC Due to CGMP Deviations: Thyroid...

The Issue: CGMP Deviations: Thyroid Powder has inconsistent levels of the active...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2018· Akorn, Inc.

Recalled Item: Ethosuximide Capsules Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2018· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Lipase Recalled by Beckman Coulter Inc. Due to NAPQI, a...

The Issue: NAPQI, a metabolite of Acetaminophen, causes negative interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...

The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050) Recalled...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco GlutaMAX Supplement Recalled by Life Technologies, Corp. Due to Leaky...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing