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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 26041–26060 of 27,254 recalls
Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...
The Issue: Firm has received reports from customers that the small pins at the bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA AST CP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL...
The Issue: Correlation slope bias and accuracy shift
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann...
The Issue: Inorganic phosphorus assays using System Diluent Lot 155599 may not product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a risk of lost images during examination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTRA C200 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by...
The Issue: A particular component may not have been fitted during the installation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The...
The Issue: RADIOMETER became aware that some membranes may have enzyme residue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...
The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...
The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a...
The Issue: The color code on label conflicts with the liner size (liner size 24 should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSX PROXIMATE Skin Staple Extractor Recalled by Ethicon Endo-Surgery Inc Due...
The Issue: Damage to the packaging may have compromised the sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) product Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling all lots of Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Repeater Pump Recalled by Baxa Corporation Due to The firm is issuing a...
The Issue: The firm is issuing a field correction to the operators manual included with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: West Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150...
The Issue: The firm recalled due to higher reactivity with some samples in the effected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.