Por fullct fem st 20x200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Check against the official notice below — it lists the full affected range.
Zimmer Biomet Inc. initiated a field action on February 28, 2017, for sterile-packaged orthopedic implants (specifically knee, hip, and nail fixation devices) in two different package configurations. The recall was triggered by failures in packaging design verification tests. Approximately 9,867 units were affected, specifically Item Number 00784302008 with lot numbers expiring before July 2026.
The affected implants were distributed worldwide, including throughout the United States and in numerous countries including Canada, Mexico, Brazil, Australia, Japan, and many others. The record does not specify a remedy for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
Reason for recall: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures. Distribution: Worldwide Distribution - US (nationwide) Foreign: Argentina, Australia, Belgium, Brazil, Bridgend Wales, Canada, Chile, Colombia, Dominican Republic, England, Eschbach, France, India, Italy, Japan, Jordan, Korea, Malaysia, Mexico, Netherlands, Nicaragua, Panama, Peru, Russia, Saudi Arabia, Singapore, Spain, Switzerland, Taiwan, Thailand Quantity: 9867 Lot/code info: Item Number: 00784302008, Lot Number Expiry Date Before: July 2026
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.