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. 961 recalls have been distributed to Alaska in the last 12 months.
Showing 30141–30160 of 46,762 recalls
Recalled Item: Travoprost Ophthalmic Solution USP Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Lack of Assurance of Sterility; damage to the internal portion of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alligator Retrieval Device The device is intended for use in Recalled by...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...
The Issue: The device defect is a positive bias of up to 20% relative to the currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...
The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm Recalled...
The Issue: The Drager Pendula spring arm device has a set of screws located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.