Every recalls & safety alerts report published for Virginia, newest first.
The FDA has terminated the Class II recall of 78 Halyard TOTAL JOINT kits distributed in Mississippi and Texas, saying the labeling failed to identify natural rubber latex in a component.
The FDA has terminated the Class II recall of 45 Halyard DaVinci TruCustom bundles over a labeling deficiency, meaning the agency considers the action carried out.
The FDA's enforcement report lists a Class II recall of Halyard TOTAL JOINT kits distributed in Mississippi and Texas because the labeling does not identify natural rubber latex in a component.
The FDA reports an ongoing Class II recall of ERIDANOUS Greek Style Shortbread Cookies due to undeclared wheat, soy, milk, eggs, and tree nut (coconut).
FDA classifies recall as Class II; product may contain undeclared wheat, soy, milk, eggs, and coconut.
AVID Medical, Inc. recalls 40 surgical kits after a component was subjected to ethylene oxide sterilization, contrary to manufacturer recommendation.
An ongoing Class I recall of Ashfiat Alharamain Energy Support due to undeclared tadalafil covers 1,052 units distributed nationwide.
An ongoing Class I recall covers 5168 AVID Medical convenience kits over particulate contamination in a component manifold. The FDA enforcement record lists no lot or serial numbers, so facilities cannot screen stock by code.
AVID Medical, Inc. initiated the ongoing recall on May 19, 2026, according to the FDA's enforcement report.
An FDA enforcement report classifies the ongoing recall as Class II, the agency's middle risk category.