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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 3086130880 of 48,770 recalls

Medical DeviceOctober 26, 2016· 3M Company - Health Care Business

Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...

The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...

The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...

The Issue: Disengaged screw head could potentially not be retained in the Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Depuy Orthopaedics Inc.

Recalled Item: ACTIS Flex Reamers SZ 0/1 Recalled by Depuy Orthopaedics Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary recall for all lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...

The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Trumpf Medical Systems, Inc.

Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...

The Issue: Trumpf has identified six incidents of pinched cables.

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROLET MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: AZUPHEN MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: URAMIT MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Hyolev MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Indiomin MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2016· Domain Surgical, Inc.

Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...

The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2016· Akorn Inc

Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...

The Issue: Subpotent Drug: concentration of product is less than labeled amount.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2016· Centurion Medical Products Corporation

Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...

The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Recovery of Incorrect Isocenter -operational change

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

Class II — Potential Health HazardOngoing