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. 2,279 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,279 in last 12 months

Showing 4434144360 of 48,770 recalls

DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: NeoCitran Extra Strength Non-Drowsy Cold & Sinus (acetaminophen 650 mg...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2013· Invacare Corporation

Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...

The Issue: There is a possibility of elevated temperatures in the seat pad. In...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2013· Hospira Inc.

Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...

The Issue: Hospira has received reports of customers experiencing air-in-line alarms...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2013· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2013· Nanosphere, Inc.

Recalled Item: Verigene BC-GN Kit (Catalog number 20-005-021) Recalled by Nanosphere, Inc....

The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2013· Nanosphere, Inc.

Recalled Item: Verigene BC-GP Kit (Catalog number 20-005-018) Recalled by Nanosphere, Inc....

The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2013· Advance Pharmaceutical Inc

Recalled Item: ENTERIC COATED ASPIRIN (NSAID) Recalled by Advance Pharmaceutical Inc Due to...

The Issue: Labeling: Label Mix-Up: A complaint from a pharmacist was received that the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 16, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...

The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· PIONEER SURGICAL TECHNOLOGY, INC.

Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...

The Issue: The affected fixed rod holders did not allow the instrument to lock down on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing