Cytoplast Titanium-Reinforced Posterior Singles Membrane A… — Class II medical device recall Z-0113-2017
Terminated recall by Osteogenics Biomedical, Inc., reported 2016-10-26. The device has the potential to be packaged in the wrong product box.
| Recall number | Z-0113-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Osteogenics Biomedical, Inc., Lubbock, TX, United States |
| Recall initiated | 2016-09-07 |
| Classified | 2016-10-18 |
| Reported by FDA | 2016-10-26 |
| Terminated | 2016-12-23 |
| Countries outside the US | CA, CO, EC, GB, IN, JP, VE |
| Quantity | 32 boxes |
| Reason classes | labeling |
| Lot numbers | 47295 |
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.
Reason for recall
The device has the potential to be packaged in the wrong product box.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0113-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.