Class II — Flower Orthopedics Corporation
| Recalling firm | FLOWER ORTHOPEDICS CORPORATION |
|---|---|
| Registered facility | FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The product is being recalled due to incidence and reports of the product breaking during surgery. |
| Product | Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set. |
| Quantity | N/A |
| Distribution | Distributed throughout the United States |
| Initiated | 2016-12-22 |
| Classified | 2017-01-28 |
| Terminated | 2017-11-27 |
| Recall number | Z-1113-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Flower Orthopedics Corporation (Z-1113-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76156/
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