Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 4078140800 of 46,762 recalls

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
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...

The Issue: The recalling firm determined that visual inspections of the fork joints...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...

The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...

The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· Baxter Corporation Englewood

Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...

The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

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

Class III — Low RiskOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

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

Class III — Low RiskOngoing
Medical DeviceNovember 29, 2013· EOS Imaging

Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...

The Issue: Error copying information to the clinical file and to the report when two 3D...

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

Class II — Potential Health HazardOngoing
DrugNovember 27, 2013· Wockhardt Usa Inc.

Recalled Item: Pantaprazole Sodium Delayed Release Tablets Recalled by Wockhardt Usa Inc....

The Issue: Failed Dissolution Specifications; 12 month acid dissolution test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2013· B. Braun Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9%...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2013· Humco Holding Group, Inc

Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...

The Issue: Microbial Contamination of Non-Sterile Product(s): The product was found to...

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

Class II — Potential Health HazardOngoing
Refund