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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 29481–29500 of 46,762 recalls
Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...
The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...
The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...
The Issue: Power outages causes reporting software to shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...
The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....
The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresenius 2008T Series Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: Used to make treatment plans Recalled by...
The Issue: Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Program Update Package AutoDELFIA¿ 3.0 Recalled by PerkinElmer Health...
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ Plate Processor Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFIA¿ PC with V3.0 Software Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K2 Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias with IMMULITE¿ /IMMULITE¿ 1000 Third Generation PSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.