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. 2,301 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,301 in last 12 months

Showing 4242142440 of 48,770 recalls

Medical DeviceDecember 9, 2013· ArthroCare Medical Corporation

Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...

The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.

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

Class II — Potential Health HazardOngoing
DrugDecember 6, 2013· Fresenius Kabi USA, LLC

Recalled Item: FOLIC ACID INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund
FoodDecember 6, 2013· Stuffed Foods LLC

Recalled Item: Stuffed Foods Asiago Risotto Bites Recalled by Stuffed Foods LLC Due to...

The Issue: Supplier informed manufacturer that cheese used in asiago risotto bites may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2013· HeartWare Inc

Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...

The Issue: The housing to the Pump's driveline connector became partially or fully...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2013· Bard Access Systems

Recalled Item: Titanium Single Lumen Low-Profile port Recalled by Bard Access Systems Due...

The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Bard Access Systems

Recalled Item: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Recalled by...

The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Lab Vision Corporation

Recalled Item: Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk Recalled...

The Issue: Reports that the product is not performing as expected. In house testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Merit Medical Systems, Inc.

Recalled Item: Catheter Recalled by Merit Medical Systems, Inc. Due to Merit Medical...

The Issue: Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q and Artis Q biplane systems Product Usage: Recalled by...

The Issue: There exists the possibility that during clinical operation, a breakdown of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Cusa Excel Rx Only CEM" Nosecone for CUSA¿ Excel Recalled by Integra...

The Issue: The blue COAG button on the CUSA Excel CEM nosecone could stick in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Symmetry Medical/SSI

Recalled Item: Symmetry and CODMAN brands Recalled by Symmetry Medical/SSI Due to The...

The Issue: The Quad-Lock Sterilization Container System may not maintain an effective...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic...

The Issue: Complaints were received regarding variability in recovery of QC and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Update to...

The Issue: Update to correct the possibility for patients or operators to have their...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...

The Issue: X-ray system C-arm casting may loosen and fall

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· CareFusion 303, Inc.

Recalled Item: Alaris PC unit model 8000 and 8015 with Alaris PCA Recalled by CareFusion...

The Issue: CareFusion is recalling the Alaris PC unit (model 8000 and 8015) because the...

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

Class I — Serious Health HazardOngoing
DrugDecember 4, 2013· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some units in certain...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 4, 2013· Invivo Corporation

Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...

The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...

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

Class II — Potential Health HazardOngoing