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. 2,251 recalls have been distributed to Alaska in the last 12 months.
Showing 45241–45260 of 46,762 recalls
Recalled Item: intraKID Lot 658 with a Best By date of 12/12 Recalled by Drucker Labs LP...
The Issue: After extensive testing and investigation, Drucker Labs has determined that...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...
The Issue: GE Healthcare became aware of a potential issue related to incorrect image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray...
The Issue: Mindray has identified the potential for a system leak resulting an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray A3 Anesthesia Delivery System Manufactured in China for Mindray...
The Issue: Mindray has identified the potential for a system leak resulting an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...
The Issue: Vital Images has found two potential errors in calcium score values in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progel Pleural Air Leak Sealant Recalled by Neomend Inc Due to Product was...
The Issue: Product was distributed with an incorrect expiration date. Product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS Urine BETA CrossLaps ELISA Recalled by Immunodiagnostics Systems Ltd Due...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Intact PINP Recalled by Immunodiagnostics Systems Ltd Due to It has...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...
The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QKC1692E The QKC1692E Quick Connect device connects endoscopes to the...
The Issue: STERIS has been actively seeking devices for quick connect revalidation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jaffe Bros. brand Recalled by Jaffe Brothers Due to Recall was initiated...
The Issue: Recall was initiated after firm was informed by their supplier Specialty...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent...
The Issue: Firm has received complaints from customers of "Abnormal Reaction" errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.