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 3538135400 of 48,770 recalls

DrugOctober 5, 2015· Inaffit, LLC

Recalled Item: NATUREAL BURN FAT NATURE Recalled by Inaffit, LLC Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 3, 2015· Skinny Latina LLC

Recalled Item: Skinny Latina Million Dollar Marinade Recalled by Skinny Latina LLC Due to...

The Issue: Undeclared soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 2, 2015· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cut Green Beans Recalled by General Mills, Inc Due to...

The Issue: General Mills is recalling a limited quantity of frozen Cascadian Farm Cut...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2015· Welch Allyn Inc

Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...

The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2015· C.R. Bard, Inc.

Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...

The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...

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

Class III — Low RiskOngoing
Medical DeviceOctober 1, 2015· Powers Medical Devices, LLC

Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...

The Issue: PAL unit has undergone significant technological changes since the previous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2015· Philips Electronics North America Corporation

Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...

The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...

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

Class II — Potential Health HazardOngoing
FoodOctober 1, 2015· Kontos Foods Inc.

Recalled Item: Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc....

The Issue: Kontos Falafel Mix contains undeclared wheat allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 1, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: Reporting feature times out after inactivity for more than an hour sending...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2015· O-Two Medical Technologies, Inc.

Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...

The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...

The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Erroneous low results on a small number of reagent wells. There is the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2015· Fit Firm and Fabulous

Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2015· Hospira Inc.

Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...

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

Class III — Low RiskOngoing
Refund