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. 2,536 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,536 in last 12 months

Showing 62216240 of 48,770 recalls

Medical DeviceMarch 1, 2024· Alere San Diego, Inc.

Recalled Item: Abbott Cholestech LDX Battery Kit Recalled by Alere San Diego, Inc. Due to...

The Issue: There is a potential that the Cholestech LDX battery (an external battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Randox Laboratories Ltd.

Recalled Item: Liquid Protein Calibrators. C3 and Haptoglobin liquid protein calibrators...

The Issue: The firm has realigned C3 and Haptoglobin in Liquid Protein Calibrators,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Floaters Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund