Reported Oct 26, 2016 · Terminated

Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) for use as…

Osteogenics Biomedical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Osteogenics Biomedical, Inc. · 4620 71st St · Lubbock, TX · 79424-2230

Is this the product you have?

  • 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.
Lot codes and dates
  • Lot 47295
Amount recalled
32 boxes

Why it was recalled

The device has the potential to be packaged in the wrong product box.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 23, 2016 · Data as of Sep 19, 4:46 PM UTC

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