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 14981–15000 of 46,762 recalls
Recalled Item: GE Healthcare Innova IGS 3 (GTIN 00840682147378) Recalled by GE Healthcare,...
The Issue: The IGS system can experience a single vertical line defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Enterprise Viewer - Product Usage: intended to be Recalled...
The Issue: A software defect was identified where the Image Styles defined by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Transdermal System Delivers 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for release rate testing and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Delivers 0.075 mg/day Recalled by...
The Issue: Defective Delivery System: Out of specification for release rate testing and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bueno Coffee Substitute Pecan Praline Recalled by Creative Foods Inc Due to...
The Issue: Bueno Coffee Substitute Pecan Praline Gluten-Free product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bueno Coffee Substitute Creamy Hazelnut Recalled by Creative Foods Inc Due...
The Issue: Bueno Coffee Substitute Creamy Hazelnut product contains undeclared hazelnut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...
The Issue: Impacted lot may leak inside the ARIES instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU Recalled by...
The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13...
The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Penumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Elevated rates of false positive/false negative and control failures while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer....
The Issue: Instruments were assembled and serviced using a defective lot of tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Recalled by Grace Healthcare Medical, Inc Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change...
The Issue: Compromised sterile barriers due to the Tyvek Lid not properly adhering to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits Recalled...
The Issue: Cannulated Screwdrivers may break at the driver tip along the shaft, near...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination...
The Issue: Examination data and patient name may be mixed up when printing or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UpsylonTM Y Mesh Kit with Colpassist Vaginal Positioning Device - Recalled...
The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.