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. 2,361 recalls have been distributed to Alaska in the last 12 months.
Showing 21941–21960 of 27,254 recalls
Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...
The Issue: The recommended sterilization and drying parameters are not effective to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...
The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the monitor may fail and requires a power circle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Trifurcated Ext set Recalled by Churchill Medical Systems, Inc....
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8" Standard Bore Ext Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" High Pressure Set with Bionector Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgical System Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The Wall chart has been updated because it was noted that Wall Chart (PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Double Lumen Set with Bionector Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifurcated set with check vales and Bionectors Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated Extension Set Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storm Series Electric Wheelchair. Invacare FDX Recalled by Invacare...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifircated Extension Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely-depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.