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. 2,333 recalls have been distributed to Alaska in the last 12 months.
Showing 32381–32400 of 46,762 recalls
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...
The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...
The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...
The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer complaint for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine gluconate Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PerioRx (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORIS (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Renovo Patch (Capsaicin Recalled by TMIG Inc Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Failed pH...
The Issue: Failed pH Specifications: Confirmed high out of specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...
The Issue: Incorrect expiration date was listed on the label. Correct expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Calretinin Recalled by Leica...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Calretinin when used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.