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. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2306123080 of 27,254 recalls

Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Cardiovascular Systems, Inc.

Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...

The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Elekta, Inc.

Recalled Item: MOSAIQ Recalled by Elekta, Inc. Due to When using CMA, if the user hovers the...

The Issue: When using CMA, if the user hovers the mouse pointer exactly above the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential loss of airway...

The Issue: Potential loss of airway gas measurement in the Compact Airway Gas Modules....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 4.5mm Round Fluted Bur Aggressive Sterile Product Usage: The...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 1.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 2.5mm x 3.6mm Neuro Drill Soft Touch Sterile Product Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.5mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 2.0mm Tapered Round Elite Bur Sterile Product Usage: The Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm x 3.8mm Precision Neuro Drill Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing