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. 2,272 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,272 in last 12 months

Showing 4602146040 of 48,770 recalls

Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...

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

Class III — Low RiskOngoing
FoodFebruary 14, 2013· Custom Co-Pak, LLC

Recalled Item: Garbanzo Iced Lemon Grass Ginger Tea 3 oz foil portion packs Recalled by...

The Issue: Recall is being conducted based on a finding of possible contamination by...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 14, 2013· Custom Co-Pak, LLC

Recalled Item: Long Life Premium Organic Green Tea with Lemongrass Recalled by Custom...

The Issue: Recall is being conducted based on a finding of possible contamination by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2013· Zimmer, Inc.

Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...

The Issue: The bed frame adapter assemblies may have a weak weld where the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...

The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...

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

Class III — Low RiskOngoing
DrugFebruary 13, 2013· Watson Laboratories Inc

Recalled Item: ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specification; tablet breakage while pushing through...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2013· Glenmark Generics Inc., USA

Recalled Item: Montelukast Sodium Tablets Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Chemical Contamination: The recall has been initiated based on multiple...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2013· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Dissolution Specification: This product recall is due to the product...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 13, 2013· Saratoga Therapeutics, LLC

Recalled Item: ebA*(TM) Multivitamin Supplement Recalled by Saratoga Therapeutics, LLC Due...

The Issue: The recall was initiated due to discovery of the presence of milk components...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2013· OLAAX International

Recalled Item: MAXILOSS Weight Advanced Recalled by OLAAX International Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: product contains sibutramine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is a potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...

The Issue: Philips was notified of a problem using the IntelliSpace Portal with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Integra LifeSciences Corp.

Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...

The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...

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

Class II — Potential Health HazardOngoing