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. 2,487 recalls have been distributed to Alaska in the last 12 months.
Showing 11641–11660 of 27,254 recalls
Recalled Item: Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 154335 Oxford Partial Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 184762 Knees Vanguard Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: TMJPM-1510 Microfixation Custom Made Device Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 189260 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Spin Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: The unplugging of the main cable on the monitor trolley from the X10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 183622 Vanguard Knee System PS Tibial Bearing Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 189420 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Products Item Number: 1) 110010462 RingLoc Hip System Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 141356 Regenerex Series-A Patella 3 Peg Recalled by Biomet,...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: The unplugging of the main cable on the monitor trolley from the X10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 183742 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...
The Issue: This product has been confirmed to exhibit holes in the packaging, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...
The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...
The Issue: There is potential for a white paper-type residue attached to the catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.