FDA Device recall Z-1113-2017
Cannulated Drill bit 2.0mm and 2.6 mm
- FDA Device
- Class II
- terminated
- Published 2017-02-08
On 2017-02-08 the FDA classified a Class II recall of Cannulated Drill bit 2.0mm and 2.6 mm by Flower Orthopedics, citing the product is being recalled due to incidence and reports of the product breaking during surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1113-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-12-22 |
| Published | 2017-02-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Flower Orthopedics |
| Distribution | US |
Product
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Reason
The product is being recalled due to incidence and reports of the product breaking during surgery.
Identifiers
| code_info | Device Listing: D267957 |
|---|
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-1113-2017%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.