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. 2,361 recalls have been distributed to Alaska in the last 12 months.
Showing 21841–21860 of 27,254 recalls
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...
The Issue: During an internal inspection of the production process the firm discovered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....
The Issue: Nonapproved labeling claims (Sterile)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm Recalled by Synthes,...
The Issue: The guide sleeve has the potential to jam in the Aiming Arms, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Clinicians observed debris, appearing to originate from the hemostasis valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical...
The Issue: This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobius3D Product Usage: Mobius3D software is used for quality assurance...
The Issue: Mobius3D version 1.5.0 contained a defect in software code which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...
The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...
The Issue: Device may experience loss of suction during treatment resulting in scoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...
The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.