FDA Device recall Z-1096-2016
NuOSS Cancellous Intended for use in dental surgery
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of NuOSS Cancellous Intended for use in dental surgery by Collagen Matrix, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1096-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-25 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Collagen Matrix |
| Distribution | MA |
Product
NuOSS Cancellous Intended for use in dental surgery.
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.
Identifiers
| code_info | Reference No. BM2C20010-U Lot no. BM2CU15E2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1096-2016%22
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