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. 2,435 recalls have been distributed to Alaska in the last 12 months.
Showing 15941–15960 of 27,254 recalls
Recalled Item: Dimension Vista¿ Mass Creatine Kinase (MMB) Flex¿ reagent cartridge Recalled...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ DHEA-SO4 Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE 1000 ¿ Gastrin Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...
The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi BR-MA (CA15-3) Recalled by Siemens...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ HBc IgM Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Thyroid Stimulating Hormone (TSHL) Flex¿ reagent cartridge...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Folic Acid Recalled by Siemens...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi 3g Allergy specific IgE Universal Kit...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Cyclosporine Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 TG Recalled by Siemens Healthcare Diagnostics,...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Cardiac Troponin I (CTNI) Flex¿ reagent cartridge Recalled...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to...
The Issue: Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...
The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...
The Issue: Communication-connection error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...
The Issue: Reports of product loosening or coming unscrewed from the handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...
The Issue: During continuous postmarket surveillance activities, we have noticed a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...
The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.