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. 2,440 recalls have been distributed to Alaska in the last 12 months.
Showing 16601–16620 of 46,762 recalls
Recalled Item: Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and...
The Issue: The device may detect an incorrect Heater Bag volume which may lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...
The Issue: There is a potential for the wrong patient information may be displayed in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* MULTIFUNCTION PEDAL OSSEODUO - Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* OSSEOSTAP Footcontrol - Product Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Version 5.6.1 - Product Usage: intended for Recalled...
The Issue: FUJIFILM has become aware of the possibility that certain CT studies may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN **** FOOTCTRL OSSEODOC - Product Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entellus Medical SN ******* Shaver System Foot Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments SN ******* S2 MINI FOOT Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Failed Impurities/Degradation Specifications; high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System...
The Issue: When the delivery catheter was attempted to be removed, there was an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System...
The Issue: Due to secondary deployment fiber being attached to secondary deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO Absorbable Suture anchors Recalled...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 W. UB COBRAID BLUE-Absorbable Suture anchor Product Number:...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO- Absorbable Suture anchors Recalled...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA HA 5.5MM W/ NEEDLES- Absorbable Suture anchor Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.