Data Foundry

Medical device recalls 2015

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 numberZ-1314-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmFlower Orthopedics Corporation, Horsham, PA, United States
Recall initiated2015-02-16
Classified2015-03-24
Reported by FDA2015-04-01
Terminated2015-08-06
DistributedCA, FL, IL, KY, NY, OK, PA, TX, VA
Quantity901
Model numbers114, 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

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1314-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

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.