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. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2504125060 of 27,254 recalls

Medical DeviceMay 20, 2013· Olympus America Inc.

Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...

The Issue: There is a possibility that the pump head was not shipped in the locked...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...

The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· RF Technologies, Inc.

Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....

The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· SpineFrontier, Inc.

Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...

The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· The Standing Company

Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...

The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Cincinnati Sub-Zero Products Inc

Recalled Item: Blanketrol III Data Export Software Version 1.10 The Blanketrol III Recalled...

The Issue: During a customer inquiry regarding a beta version of the Bill Data Export...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Sysmex America Inc

Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...

The Issue: The data printed on the thermal printer may omit a digit or decimal point in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Maytex Corp

Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...

The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...

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

Class II — Potential Health HazardOngoing