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. 2,524 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,524 in last 12 months

Showing 75417560 of 13,366 recalls

DrugOctober 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Famotodine has an out of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2017· Leading Pharma, LLC

Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2017· United Pharmacy

Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...

The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to...

The Issue: Subpotent Drug: low out of specification results.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Sandoz Inc

Recalled Item: Ampicillin for Injection Recalled by Sandoz Inc Due to Labeling: Missing...

The Issue: Labeling: Missing Label: customer complaint that some vials of ampicillin...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline I&D Tray Kit Recalled by Medline Industries Inc Due to Subpotent...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline CC Drawer 4 IV Circulation Pack Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline DC Line Kit Recalled by Medline Industries Inc Due to Subpotent...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline CNTRL Line Removal Kit Scripps. Packaged in USA for Medline...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Staple Remover Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Incision and Drainage Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Incision and Drainage Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund