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 31041–31060 of 46,762 recalls
Recalled Item: cobas p 312 Pre-Analytical System calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 Modular Analyzer Series c8000 Recalled by Roche Diagnostics...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 Post-Analytical Unit calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 512 Pre-Analytical Instrument calculator/data processing module...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche COBAS INTEGRA 800 /800 CTS Analyzer Analyzer Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 612 Pre-Analytical Instrument calculator/data processing module...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSD 800A Aliquoting System calculator/data processing module Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...
The Issue: Microbial contamination of Non-Sterile Products; positive findings of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol Recalled...
The Issue: Failed Content Uniformity Specifications: out of specification test result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.