Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker Craniomaxillofacial Division Due to Potential for implant damage, implant cracking off/breaking intra-operatively.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Craniomaxillofacial Division directly.
Affected Products
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.
Quantity: 1051
Why Was This Recalled?
Potential for implant damage, implant cracking off/breaking intra-operatively.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Craniomaxillofacial Division
Stryker Craniomaxillofacial Division has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report