Recall archive
3 recalls · page 1 of 1
Reported Oct 22, 2025
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
Matched: Brand · Product · Product details — Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk…
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
Matched: Brand · Reason for recall — There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards…
9 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
Matched: Brand · Product · Product details — Manufacturing flaw in the sterile barrier system
20 more products in this recall
FDA (openFDA device enforcement)
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