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. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2314123160 of 48,770 recalls

DrugNovember 6, 2018· Breckenridge Pharmaceutical, Inc.

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...

The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2018· L. Perrigo Company

Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...

The Issue: Presence of foreign substance: Product found to contain metal particles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· COVIDIEN LLC

Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...

The Issue: The product was released into commercial distribution while subject to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Bausch & Lomb Surgical, Inc.

Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...

The Issue: Cosmetic imperfections on the surface of some lenses.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...

The Issue: Potential for external blood leaks from the dialyzer header

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

Class II — Potential Health HazardOngoing
DrugNovember 5, 2018· Kadesh International

Recalled Item: puriton EYE RELIEF DROPS Recalled by Kadesh International Due to...

The Issue: Non-Sterility: Product manufactured under non-sterile production conditions.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 5, 2018· ConAgra Foods, INc.

Recalled Item: Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail Recalled by...

The Issue: positive finding of Salmonella in a retail sample

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 5, 2018· ConAgra Foods, INc.

Recalled Item: Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail Recalled by...

The Issue: positive finding of Salmonella in a retail sample

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 5, 2018· ConAgra Foods, INc.

Recalled Item: Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail Recalled by...

The Issue: positive finding of Salmonella in a retail sample

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 5, 2018· ConAgra Foods, INc.

Recalled Item: Duncan Hines Classic Classic White cake mix 15.25oz. 12 retail Recalled by...

The Issue: positive finding of Salmonella in a retail sample

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund