FDA Device recall Z-2452-2015
3.0/4.0 Cannulated Drill Bit
- FDA Device
- Class II
- terminated
- Published 2015-09-02
On 2015-09-02 the FDA classified a Class II recall of 3.0/4.0 Cannulated Drill Bit by Trilliant Surgical, citing the cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2452-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-20 |
| Published | 2015-09-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Trilliant Surgical |
| Distribution | US |
Product
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for single use only.
Reason
The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through.
Identifiers
| code_info | Lot 1363-01 |
|---|
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-2452-2015%22
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