Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) Recalled by Osteogenics Biomedical, Inc. Due to The device has the potential to be packaged...
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 Osteogenics Biomedical, Inc. directly.
Affected Products
Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) for use as a space-making barrier in the treatment of periodontal bone defects.
Quantity: 32 boxes
Why Was This Recalled?
The device has the potential to be packaged in the wrong product box.
Where Was This Sold?
Worldwide Distribution - US Distribution and to the countries of : Colombia, Venezuela/Ecuador, Japan, India, Canada, and UK.
About Osteogenics Biomedical, Inc.
Osteogenics Biomedical, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report