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 13821–13840 of 27,254 recalls
Recalled Item: LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr...
The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Recalled by...
The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Potential loose cable connections on the reagent cooler, which could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...
The Issue: The manufacturer received complaints that customers were attempting to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...
The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...
The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...
The Issue: Dental adaptor does not conform to specifications. The dental coupling of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...
The Issue: There is no warning in the Elekta Unity manual for the administration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.