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. 1,061 recalls have been distributed to Alaska in the last 12 months.
Showing 2541–2560 of 46,762 recalls
Recalled Item: Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit. Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The...
The Issue: Potential crack in the female connector located on the Heat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHENYLephrine HCl in 0.9% Sodium Chloride Recalled by Denver Solutions, LLC...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine HCl 50mg per 5mL (10 mg per mL) Recalled by Denver Solutions, LLC...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: dexmedeTOMIDine HCl PF Recalled by Denver Solutions, LLC DBA Leiters Health...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost powder Recalled by Medisca Inc. Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide 50 mg per 5mL (10mg per mL) Recalled by Denver Solutions,...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72...
The Issue: During routine preventative maintenance checks, it was revealed that carbon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Guidewire Guidewires are intended for use in Recalled by Galt Medical...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional Coaxial Dilator Recalled by Galt Medical Corporation...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular Lens. enVista Envy IOL Recalled by Bausch & Lomb Surgical, Inc....
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.