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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 14041–14060 of 27,254 recalls
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...
The Issue: The firm became aware of the potential for the products' sterile pouch to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...
The Issue: Packaged with an incorrect size inner cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...
The Issue: The optional Vacuum Unit may stop working and display the failure message...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...
The Issue: Incorrect needle length and gage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.