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Osteogenics Biomedical, Inc. recalls Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) for use
Recalled October 26, 2016 · FDA recall Z-0113-2017 · Osteogenics Biomedical
Hazard
The device has the potential to be packaged in the wrong product box. · FDA Class II
Units
32 boxes
Sold at
Worldwide Distribution - US Distribution and to the countries of : Colombia, Venezuela/Ecuador, Japan, India, Canada, and UK.
Description
The device has the potential to be packaged in the wrong product box.
Product
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.
Manufacturer(s)
Osteogenics Biomedical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →