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. 2,366 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,366 in last 12 months

Showing 2594125960 of 48,770 recalls

Medical DeviceMarch 2, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has determined that there is a potential for incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Randox Laboratories Ltd.

Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...

The Issue: Randox has now released further steps to avoid contamination of the Lipase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
DrugFebruary 28, 2018· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Biomet, Inc.

Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...

The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Blemish Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund