Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants Recalled by Stryker Craniomaxillofacial Division Due to Potential for implant deformation, implant mechanical stability too...
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 BARRIER Sheets Orbital Floor Implant 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 deformation, implant mechanical stability too low, loss of barrier adhesion intra-operatively, 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