NuOSS Cancellous Intended for use in dental surgery — Class II medical device recall Z-1096-2016
Terminated recall by Collagen Matrix Inc, reported 2016-03-23. On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to
| Recall number | Z-1096-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Collagen Matrix Inc, Franklin Lakes, NJ, United States |
| Recall initiated | 2015-08-25 |
| Classified | 2016-03-11 |
| Reported by FDA | 2016-03-23 |
| Terminated | 2016-05-11 |
| Quantity | 171 units |
| Lot numbers | BM2CU15E2 |
Product
NuOSS Cancellous Intended for use in dental surgery.
Reason for recall
On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an incorrect size.
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-1096-2016. 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.