FDA Device recall Z-0823-2022
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects
- FDA Device
- Class II
- ongoing
- Published 2022-03-30
On 2022-03-30 the FDA classified a Class II recall of NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects by Ace Surgical Supply, citing nuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for oral wounds) rather than NuOss Collagen Block, may result in suboptimal bone repair.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0823-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-02-02 |
| Published | 2022-03-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ace Surgical Supply |
| Distribution | US |
Product
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
Reason
NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for oral wounds) rather than NuOss Collagen Block, may result in suboptimal bone repair
Identifiers
| code_info | Lot Number: BMBU21A1 Exp. Date: 2024-03-31 UDI: 00614950007264 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0823-2022%22
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