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 461–480 of 27,254 recalls
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...
The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...
The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full...
The Issue: Affected gowns have the incorrect expiration date on the product packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. CAMHB W/LHB Recalled by Remel, Inc Due to Products may contain...
The Issue: Products may contain contamination, which may result in a darker or brown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker CranialMask Tracker is a single-use device consisting of...
The Issue: When the device is activated during surgery, the device software issues an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.