Class II — Collagen Matrix Inc
| Recalling firm | COLLAGEN MATRIX, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | NuOSS Cancellous Intended for use in dental surgery. |
| Quantity | 171 units |
| Distribution | US Distribution to the state of : MA |
| Initiated | 2015-08-25 |
| Classified | 2016-03-11 |
| Terminated | 2016-05-11 |
| Recall number | Z-1096-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Collagen Matrix Inc (Z-1096-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73222/
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