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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 15421–15440 of 46,762 recalls
Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Romidepsin Injecton Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurity/Degradation Specifications: Out-of-specifications results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensis/ Sensis Vibe Hemo systems with VD12A software as follows: Recalled by...
The Issue: Due to the configuration of certain Windows Service Permissions within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 45 mm Recalled...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 30 mm Recalled...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to ROi CPS, LLC has become aware, through...
The Issue: ROi CPS, LLC has become aware, through a vendor issued urgent medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: p-Chip Wand Reader Recalled by p-Chip Corporation Due to The laser operation...
The Issue: The laser operation might fall under a higher laser class.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad Recalled by...
The Issue: Pump Module keypad lifting, and Fluid ingress could result in 1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console Recalled by...
The Issue: An electrical component within the system controller module of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information...
The Issue: Patient related messages created in RayCare 3B, RayCare 4A will be lost when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed...
The Issue: SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Recalled by A-S Medication Solutions LLC. Due to Labeling:...
The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH...
The Issue: Failed pH specifications: Out of Specification pH results for 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Valentine Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Autumn Assorted Treat Toppings Sprinkles Recalled by Wilton...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.