FDA Device recall Z-2191-2020
OSTEOVATION RMX 10 CC Injectable
- FDA Device
- Class II
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of OSTEOVATION RMX 10 CC Injectable by Osteomed, citing incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2191-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-02 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Osteomed |
| Distribution | US |
Product
OSTEOVATION RMX 10 CC Injectable. REF/UDI: 390-6002/ /00813845021099 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Reason
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
Identifiers
| code_info | LOT 1127902, 1129603, 1132560, 1134444, 1137073, 1141342 and 1142084 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2191-2020%22
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