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 | Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure |
| Product | Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with solid 2.7mm screws and can be used with any the Flower Small and Medium Implant Set Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: DBK 027 |
| Quantity | 3 units |
| Distribution | Arizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas Virginia |
| Initiated | 2021-09-01 |
| Classified | 2021-10-13 |
| Terminated | 2023-02-16 |
| Recall number | Z-0113-2022 |
| 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-0113-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88669/
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