FDA Device recall Z-1768-2014
Stryker 5.0mm Barrel Bur Sterile
- FDA Device
- Class II
- terminated
- Published 2014-06-18
On 2014-06-18 the FDA classified a Class II recall of Stryker 5.0mm Barrel Bur Sterile by Stryker Instruments Div, citing there may be missing notches, partial notches or no notches at all in some Cutting Accessories that are used with the Elite" Attachments.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1768-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-22 |
| Published | 2014-06-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Instruments Div |
| Distribution | US |
Product
Stryker 5.0mm Barrel Bur Sterile
Reason
There may be missing notches, partial notches or no notches at all in some Cutting Accessories that are used with the Elite" Attachments.
Identifiers
| code_info | Part Number 5820-17-50, Lot Number 13345017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1768-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.