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 16021–16040 of 46,762 recalls
Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 3"x100'. One roll per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 4"x100'. One roll per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos MIC Panel Type 34 - Product Usage: For Recalled by Beckman...
The Issue: Due to a customer report and internal investigation, it was confirmed that a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...
The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...
The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neostigmine Methylsulfate PF Inj. 5 mg/5 mL Recalled by US Compounding Inc...
The Issue: Labelling: Missing label.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific lots...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Fixed Lateral Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.