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 26341–26360 of 27,254 recalls
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 PN 0000280010 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 LAS PN 0000280030 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The...
The Issue: Ethicon Endo-Surgery initiated this voluntary global recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...
The Issue: May emit a continuous high priority alarm and the ventilator may stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...
The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an...
The Issue: Cartridges are leaking. The leaking is observed when opening the wrapper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...
The Issue: Devices leaking at the Y-site
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the foot switch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...
The Issue: Customers were not following the labeled assay procedure. This was due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...
The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...
The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...
The Issue: The firm initiated a recall after complaint investigations revealed that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...
The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.