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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 2301–2320 of 46,762 recalls
Recalled Item: Celecoxib Capsules Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indomethacin Extended-Release Capsules USP Recalled by KVK Tech, Inc. Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK Tech, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: A software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Description/: MNA-420 ENC -H/K9303320 Recalled by Barco N.V. Due to...
The Issue: Cathode ray tube display system encoders and decoders have same MAC address;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope...
The Issue: The replacement rechargeable batteries inserted into the Welch Allyn...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW Nutritional Yeast Powder Recalled by Now Foods Due to regular yeast was...
The Issue: regular yeast was inadvertently packaged as nutritional yeast
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD Pyxis Product Name / UDI-DI code / Catalog No. Recalled by CareFusion...
The Issue: Antivirus software was not consistently installed on impacted devices during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...
The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...
The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Coil System /UDI-DI codes: PRES0153CXPPLT 00810068567311...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System /UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Alembic Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Valeda Light Delivery System Product Name: Light Based Recalled...
The Issue: U.S. customers were shipped devices that were configured for the European...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer C11137 Recalled by Beckman Coulter,...
The Issue: Analyzer has calibration issues where curves switched from passed to failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.