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 2916129180 of 48,770 recalls

Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Teleflex Medical

Recalled Item: PE CONNECTOR 3/8 STRAIGHT 20/BX Recalled by Teleflex Medical Due to...

The Issue: Labeling: The expiration date is not stated on the labeling, there is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Flat Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Teleflex Medical

Recalled Item: INFANT 20/BX Recalled by Teleflex Medical Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Amitriptyline HCL Tablets Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Labeling: Labeled...

The Issue: Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· Akorn, Inc.

Recalled Item: IC-Green (indocyanine green for injection Recalled by Akorn, Inc. Due to...

The Issue: Product is being recalled due to low pH value.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N265) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Streptococcus Susceptibility card (AST-ST01) Recalled by...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing