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. 2,348 recalls have been distributed to Alaska in the last 12 months.
Showing 24101–24120 of 27,254 recalls
Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...
The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Recalled...
The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assembly Recalled by Intuitive Surgical, Inc. Due to Reports of friction...
The Issue: Reports of friction within certain instrument arms can interrupt smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunrise Brand Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to...
The Issue: There is a remote possibility for the plastic latch to deform over the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Monitor Suspensions that may be on the following Fluoroscopic Recalled...
The Issue: Missing screws in the overhead Video Monitor Suspension. GE discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill...
The Issue: Following a retrospective review for Baxter Daytona Complaint CR-954, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria () API Listeria is a standardized system Recalled by Biomerieux...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NH () API NH is a standardized system Recalled by Biomerieux France...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaSafe Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the VersaSafe Extension Intravascular Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 780 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent () ZYM B reagent is an Recalled by Biomerieux France Chemin De...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB) Recalled by Arrow...
The Issue: Potential for a leak between the catheter and the bifurcate which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...
The Issue: EOS imaging discovered during production internal testing that the X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...
The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...
The Issue: There exists a software issue associated with patient selection from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...
The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candela Laser GentleLase Pro Recalled by Candela Corporation Due to...
The Issue: Unintended single pulse maybe emitted to handpiece prior to pressing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.