FDA Device recall Z-2059-2017
Bone Dowell Harvest Tubes
- FDA Device
- Class II
- terminated
- Published 2017-05-17
On 2017-05-17 the FDA classified a Class II recall of Bone Dowell Harvest Tubes by Zimmer Biomet, citing mislabeled as 8mm tube but it is actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual 8mm subcomponent part.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2059-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-12 |
| Published | 2017-05-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | n/a |
Product
Bone Dowell Harvest Tubes
Reason
mislabeled as 8mm tube but it is actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual 8mm subcomponent part.
Identifiers
| code_info | Part Number: 900738 Lot Number (LN): 889990 |
|---|
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-2059-2017%22
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