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 54615480 of 48,770 recalls

Medical DeviceMay 13, 2024· Young Dental Manufacturing I, LLC

Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...

The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...

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

Class II — Potential Health HazardOngoing
FoodMay 10, 2024· Wehah Farms

Recalled Item: Lundberg Family Farms Sustainable Wild Blend Gourmet Rice Recalled by Wehah...

The Issue: Product may contain foreign object that appears to be of rodent origin.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 10, 2024· Healthwest Minerals, Inc. dba Mt. Capra Products

Recalled Item: Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. Recalled by...

The Issue: The Goat Milk Formula Recipe Kit has been sold and marketed as infant...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Front label states 100 Tablets instead...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back label states Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore Arcadia H Recalled by LEICA BIOSYSTEMS NUSSLOCH GMBH Due to...

The Issue: An issue with safe usage of the device was identified whereby toxic smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Ascenda Intrathecal Catheter Recalled by Medtronic Neuromodulation...

The Issue: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL (poliglecaprone 25) Suture - Intended for use in general Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing