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 14001–14020 of 46,762 recalls
Recalled Item: Spironolactone Ophthalmic Solution 0.005 mg/mL Recalled by Prescription Labs...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X RATED HONEY FOR MEN Recalled by Phe Inc Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EVIS EXERA BF-XT160 Bronchofibervideoscope Recalled by Olympus Corporation...
The Issue: A gluing step was not performed during the manufacturing of the affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-P180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1T180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-Q180-AC EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XP60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1T60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XP160F EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C40 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-P60 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A Recalled by...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with syngo.via VB30 Recalled by Siemens Medical...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08 Recalled...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...
The Issue: Revised Instructions for Use: Potential for specimens from patients with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.