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 15061–15080 of 46,762 recalls
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PremierZen Black 5000 Recalled by Hyobin LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triple SupremeZen Plus 3500 Recalled by Hyobin LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Extreme 3000 Recalled by Hyobin LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Recalled by Philips Respironics, Inc. Due to Certain devices were...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Certain devices...
The Issue: Certain devices were built with motor assemblies that could contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeverEdge Contrast Injector: 35 cc syringe with ISO 594 female Recalled by...
The Issue: The firm received a complaint regarding particulate found in the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE VIBIL Biliary Endoprosthesis: stents Recalled by W.L. Gore &...
The Issue: The Gore post market surveillance team received a complaint that a GORE¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starwest Botanicals Item#: 209617-34 Recalled by Starwest Botanicals, Inc...
The Issue: Presence of E. coli species
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg Laser Applicator Non-cooled Recalled by CLINICAL LASERTHERMIA...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...
The Issue: Inability for the user to inject the paste from the syringe into the target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.