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 2936129380 of 48,770 recalls

Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P629) 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 Negative Susceptibility card (AST-N350) 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 Positive Susceptibility card (AST-P603) 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 Negative Susceptibility card (AST-N211) 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 Negative Susceptibility card (AST-N293) 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· Acumed LLC

Recalled Item: The Acumed Slide-Loc Anatomic Radial Head System is intended for Recalled by...

The Issue: The firm initiates a voluntary removal and discontinue marketing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· EBI Patient Care, Inc.

Recalled Item: 10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion...

The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 20, 2017· EBI Patient Care, Inc.

Recalled Item: 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a Recalled...

The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 20, 2017· Almore International Inc

Recalled Item: Microfil Composite Instruments are packaged in an unsealed plastic sleeve...

The Issue: Microfil Composite Instruments were distributed with a sterile symbol on...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2017· Olympus Corporation of the Americas

Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...

The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.

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

Class II — Potential Health HazardOngoing
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 18 mg pellet Recalled by Qualgen Due to CGMP deviations- Lack of...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 12.5 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Gentell, Inc

Recalled Item: Shield and Protect Moisture Barrier Cream Recalled by Gentell, Inc Due to...

The Issue: GMP Deviations; product may not meet cGMP requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 25 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 10 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 20 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 6 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 15 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2017· Qualgen

Recalled Item: Estradiol 22 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...

The Issue: CGMP deviations- Lack of Quality Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: HYDROXO-B12 5ML PBF MDV (CALIF) 10MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund