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. 2,384 recalls have been distributed to Alaska in the last 12 months.
Showing 18641–18660 of 27,254 recalls
Recalled Item: Roche COBAS INTEGRA c111 Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: cobas c 111 analyzers (catalog numbers 04777433001 and 04528778001) with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The surgical table is a stand alone unit. Three (3) Recalled by Schaerer...
The Issue: The floor locking cylinders contained in the base of the Schaerer 7300 model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heater Cooler Unit Usage: The Heater-Cooler Unit (HCU 30) supplies Recalled...
The Issue: There is the potential for contaminated water to enter parts of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is...
The Issue: Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waste Management Kit. Catalog Number K10-04381AP Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential...
The Issue: Potential risk associated with corrosion demonstrated on the distraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product...
The Issue: There is a potential for a component failure of the device which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog...
The Issue: O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD79b PE (ASR) Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: CD79b (SN8) PE is contaminated with a FITC conjugate of unknown antigenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...
The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Product was found to contain excess residual levels of hydrogen peroxide.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...
The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.