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. 2,417 recalls have been distributed to Alaska in the last 12 months.
Showing 17981–18000 of 27,254 recalls
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...
The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...
The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System - C-Spine Coil Recalled by Hitachi Medical Systems...
The Issue: The customer indicated that the coil balun was hot to the touch when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: The company received a customer complaint for the inability to calibrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...
The Issue: There is a possibility for data to be stored under the wrong patient on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...
The Issue: packaging of some femoral components was incorrectly labeled as either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issue on strain categorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.