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. 2,463 recalls have been distributed to Alaska in the last 12 months.
Showing 14361–14380 of 27,254 recalls
Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...
The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...
The Issue: Screw is missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...
The Issue: An incorrect test result for a single analyte may have been reported for up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing, LLC Due to...
The Issue: packaging error; An internal QA inspection revealed that a incorrect healing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...
The Issue: Potential metal burrs in the holes of the device preventing the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more...
The Issue: False resistant results for Streptococcus anginosus and Streptococcus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip Recalled...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage:...
The Issue: Inspection process at the manufacturer found nonwoven material was used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.