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 2596125980 of 48,770 recalls

FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Ayurvedic 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
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: French Rose Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

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
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Green Tea Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

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
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Lemongrass Facial Polish with Oats Recalled by Plant Devas Inc Due to FDA...

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
FoodFebruary 27, 2018· Plant Devas Inc

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

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
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Clay Mask Kit Recalled by Plant Devas Inc Due to FDA Office of Colors and...

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
FoodFebruary 27, 2018· Plant Devas Inc

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

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
Medical DeviceFebruary 27, 2018· Integrity Implants Inc.

Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...

The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Radiometer Medical ApS

Recalled Item: AQURE Recalled by Radiometer Medical ApS Due to There is a potential problem...

The Issue: There is a potential problem relating to the AQURE System, versions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Adult/Pediatric Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD has...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2018· Mckesson Packaging Services

Recalled Item: RANITIDINE Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2018· Paddock Laboratories, LLC.

Recalled Item: Evamist (estradiol transdermal spray) Recalled by Paddock Laboratories, LLC....

The Issue: Defective Delivery System: Potential that cracks in the vial neck near the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2018· Genesee BioMedical, Inc.

Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...

The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Beaver-Visitec International Inc.

Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...

The Issue: Products were packaged with incorrect labeling,

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

Class II — Potential Health HazardOngoing
DrugFebruary 23, 2018· AstraZeneca Pharmaceuticals LP

Recalled Item: Lynparza (olaparib) capsules 50 mg Recalled by AstraZeneca Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications; elevated levels of quality...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Thyroid Resilience 120 count bottle packaged in an amber plastic Recalled by...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund