Cannulated Drill bit 2 — Class II medical device recall Z-1113-2017
Terminated recall by Flower Orthopedics Corporation, reported 2017-02-08, distributed nationwide. The product is being recalled due to incidence and reports of the product breaking during surgery.
| Recall number | Z-1113-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flower Orthopedics Corporation, Horsham, PA, United States |
| Recall initiated | 2016-12-22 |
| Classified | 2017-01-28 |
| Reported by FDA | 2017-02-08 |
| Terminated | 2017-11-27 |
| Distributed | Nationwide (US) |
Product
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Reason for recall
The product is being recalled due to incidence and reports of the product breaking during surgery.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1113-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.