Osteogenics Biomedical, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0113-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: September 7, 2016

Date Posted: October 26, 2016

Recall Number: Z-0113-2017

Event ID: 75119

Reason for Recall:

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

Status: Terminated

Product Quantity: 32 boxes

Code Information:

Lot 47295

Distribution Pattern:

Worldwide Distribution - US Distribution and to the countries of : Colombia, Venezuela/Ecuador, Japan, India, Canada, and UK.

Voluntary or Mandated:

Voluntary: Firm initiated