FDA Designates IsoTis OrthoBiologics Recall as Class II
On August 5, 2026, the FDA classified the ongoing recall of 98 bone graft extender products as a Class II action.
Recalls & Safety Alerts in Irvine, California
Every recalls & safety alerts report published for Irvine, California, newest first.
FDA Records Class II Recall of 13 Brain Flow-Diverter Implants Over Swapped Length Labeling
An FDA enforcement report lists Micro Therapeutics, Inc. recalling Pipeline Flex Embolization Devices whose labeled implant length does not match the implant inside; the action is listed as ongoing.
FDA Records Class II Recall of Six Brain Flow-Diverter Implants Over Mislabeled Lengths
An FDA enforcement report lists Micro Therapeutics, Inc. as recalling six units of the Pipeline Flex Embolization Device with Shield Technology after devices were labeled with the wrong implant length; the action is listed as ongoing.