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 | Locking pegs were not locking during distal radius procedures. There has been one (1) report of revision surgery scheduled to remove a loosened peg. |
| Product | Variable Angle Locking Peg, D:1.8mm x L:14.0mm; Variable Angle Locking Peg, D:1.8mm x L:16.0mm, Variable Angle Locking Peg, D:1.8mm x L:18.0mm; Variable Angle Locking Peg, D:1.8mm x L:20.0mm; Variable Angle Locking Peg, D:1.8mm x L:22.0mm, Variable Angle Locking Peg, D:1.8mm x L:24.0mm; Variable Angle Locking Peg, D:1.8mm x L:26.0mm. The locking pegs are intended to be used in conjunction with the Flower Orthopedics Distal Radius Plate for osteosynthesis of the radius bone. |
| Quantity | 901 |
| Distribution | Distributed in the states of VA, TX, IL, OK, PA, CA, NY, KY, and FL. |
| Initiated | 2015-02-16 |
| Classified | 2015-03-24 |
| Terminated | 2015-08-06 |
| Recall number | Z-1314-2015 |
| 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-1314-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70578/
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