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 26281–26300 of 27,254 recalls
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...
The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...
The Issue: The firm recalled the device after learning of a possible deviation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...
The Issue: There is a potential for epistaxis during use of the Disposable General...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...
The Issue: Shipped with incorrect software
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...
The Issue: The recall was initiated because Karl Storz has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275...
The Issue: Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to On August...
The Issue: On August 15, 2012, Sorin informed consignees via letter of changes made to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...
The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation found that the current design of the product allows the...
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: 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 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: 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: 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.