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. 2,344 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,344 in last 12 months

Showing 3428134300 of 48,770 recalls

DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Black Storm Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Weekend Prince Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Real Skill Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Mojo Risen Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Germany Niubian Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Herb Viagra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bigger Longer More Time More Sperms Recalled by R Thomas Marketing, LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Super Hard Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: African Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Hard Ten Days Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 8, 2016· Perrigo Company PLC

Recalled Item: Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan...

The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 8, 2016· Perrigo Company PLC

Recalled Item: Guaifenesin Grape liquid 100 mg/5 mL Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2016· Natus Medical Incorporated

Recalled Item: Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator. Recalled...

The Issue: NatalCare LX Incubators were manufactured using a defective oval port hinge...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· Cook Inc.

Recalled Item: Kopans Breast Lesion Localization Needle The Kopans Breast Lesion...

The Issue: Product potentially exposed to body fluids during processing. Potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be Recalled by...

The Issue: Increased punch height, causing a 0.063 in (1.6 mm) gap between the trial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This...

The Issue: Olympus America Inc is conducting a voluntary removal/corrective action of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· Philips Medical Systems

Recalled Item: DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0...

The Issue: In DS/US proton planning, there is a correction factor used internally to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· BioMerieux SA

Recalled Item: API ZYM Bx2 () Product Usage: ZYM B reagent Recalled by BioMerieux SA Due to...

The Issue: Discrepant identification results related to API identification strips....

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

Class II — Potential Health HazardOngoing