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. 1,027 recalls have been distributed to Alaska in the last 12 months.
Showing 16121–16140 of 46,762 recalls
Recalled Item: DePuy Synthes 11.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisafe Distal Duck Kit and Duck Bag Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that certain lots of diluted 4-Zyme may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM 50-001-01 Injectate Kit Recalled by Lidco Ltd Due to The expiration date...
The Issue: The expiration date on labeling is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HVAD Pump Implant Kits Recalled by Heartware, Inc. Due to Pumps...
The Issue: Pumps manufactured with impellers from a subset of lots from a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 14.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emission Computed Tomography System Image Process System - Product Usage:...
The Issue: A software defect that has the potential to result in image misdiagnosis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...
The Issue: Dirty Lens May Cause Invalid or False Positive Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 11.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 14.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 12.5MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic Recalled by...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 10.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 16.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 16.0MM REAMER HEAD FOR RIA 2 STERILE--Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 10.0MM REAMER HEAD FOR RIA 2 Recalled by Synthes (USA)...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Areva Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: based on a Warning Letter received by the manufacturer of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Immune Boost with natural strawberry flavor Recalled by Fusion Health and...
The Issue: Marketed without an Approved NDA/ANDA: Product marketed with drug claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.