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 | Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced) |
| Product | Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201 |
| Quantity | 77 kits |
| Distribution | US Nationwide distribution in the states of AZ, CA, CO,CT, FL, IL, IN, NC, NY, NV, OH, WV, TX. |
| Initiated | 2021-09-03 |
| Classified | 2021-10-06 |
| Terminated | 2022-07-28 |
| Recall number | Z-0034-2022 |
| 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-0034-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88724/
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