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. 2,440 recalls have been distributed to Alaska in the last 12 months.
Showing 15221–15240 of 27,254 recalls
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...
The Issue: GE Medical Systems has discovered a small area on the bore surface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...
The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Chamber Temporary External Pacemaker Recalled by Medtronic Inc.,...
The Issue: A subset of Medtronic Model 53401 Single Chamber External Pulse Generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The firm has learned that some RayStation/RayPlan users have commissioned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoMed Enteral Feeding Tubes with Enteral Only Connectors Recalled by Neomed...
The Issue: Potential for the tethered plug on the hub of the NeoMed Enteral Feeding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fx SOLUTIONS CENTERED HEAD CoCr 50x19 Recalled by Fx Solutions Due to Breach...
The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Microsystems products labeled as the following: Leica M320 Microscope...
The Issue: Possible failure of screws which hold the gas spring fixation bracket in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fx SOLUTIONS OFFSET HEAD CoCr 50x20 Recalled by Fx Solutions Due to Breach...
The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Single Cytofunnel Brown Recalled by Richard-Allan Scientific Company Due...
The Issue: Mislabeled product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The firm has identified the potential for a silicone particle to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...
The Issue: Baxter r recalled this device due to the use of an incorrect plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...
The Issue: Under certain circumstances, the firmware makes it possible for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...
The Issue: Cap may be mislabeled with incorrect part number, although the correct part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.