Variable Angle Locking Peg — Class II medical device recall Z-1314-2015
Terminated recall by Flower Orthopedics Corporation, reported 2015-04-01, distributed in CA, FL, IL, KY, NY, OK, PA, TX…. Locking pegs were not locking during distal radius procedures. There has been one (1) report of revision surge
| Recall number | Z-1314-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flower Orthopedics Corporation, Horsham, PA, United States |
| Recall initiated | 2015-02-16 |
| Classified | 2015-03-24 |
| Reported by FDA | 2015-04-01 |
| Terminated | 2015-08-06 |
| Distributed | CA, FL, IL, KY, NY, OK, PA, TX, VA |
| Quantity | 901 |
| Model numbers | 114, 116, 118, 120, 122, 124, 126 |
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.
Reason for recall
Locking pegs were not locking during distal radius procedures. There has been one (1) report of revision surgery scheduled to remove a loosened peg.
Machine access
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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.