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. 2,524 recalls have been distributed to Alaska in the last 12 months.
Showing 6321–6340 of 46,762 recalls
Recalled Item: CARTO VIZIGO Bi-Directional Guiding Sheath Recalled by Biosense Webster,...
The Issue: Due to a manufacturing issue, device under process validation phase were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methocarbamol Injection Recalled by Eugia US LLC Due to Presence of...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...
The Issue: If the DIVA touch display generates touch inputs without user interaction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mariner RDX Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION Due...
The Issue: Screw heads, of pedicle screw systems, have thin lead-in thread that pose a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...
The Issue: Due to incorrect calibrations and controls, their is a potential of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluticasone Propionate Nasal Spray USP Recalled by Golden State Medical...
The Issue: CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Signia" Small Diameter Curved Tip Intelligent Reload Recalled by Covidien,...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload Recalled by...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cystatin C Calibrator - In vitro diagnostic (IVD) use in Recalled by Randox...
The Issue: Cystatin C Calibrator Series CVS 2699, is running with a negative bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Boot Assembly Recalled by Baxter Healthcare Corporation Due to Three...
The Issue: Three lots of the Boot Assembly, Traction Device are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM...
The Issue: Automated external defibrillators were shipped in their test configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oseltamivir Phosphate for Oral Suspension 6mg/ml Recalled by Amneal...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification test results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ForeverMen Natural Energy Boost Capsules Recalled by FA Online Inc Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CABTREO (clindamycin phosphate Recalled by MCKESSON CORPORATION Due to CGMP...
The Issue: CGMP Deviations: Product was stored outside labeled storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets 10mg Recalled by Micro Labs Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: Out of specification for residual solvents.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.