Peri-Loc 71829312Recalls & reported problems
Smith & Nephew, Inc. · PERI-LOC 4.5MM LOCKING COMPRESSION PLATE 12 HOLE 229MM · Class 2 · Implant
All models of Peri-Loc (102)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010527639), received between Jun 6, 2022 and Jun 6, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
1 other recall cover devices cleared under the same FDA submission (K033669, K210837); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Fracture1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 6, 2022Fracture; Fracture
IT WAS REPORTED THAT, AFTER AN INTERNAL FIXATION SURGERY PERFORMED ON (B)(6) 2021, THE PATIENT UNDERWENT A REVISION SURGERY ON 13-AUG-2021 TO REMOVE THE PERI-LOC 4.5MM LOCKING COMPRESSION PLATE 12 HOLE 229MM DUE TO FRACTURE. PATIENT UNDERWENT ANOTHER REVISION SURGERY ON 22-NOV-2021 DUE TO ANOTHER PLATE BREAKAGE.
Patient problems: Insufficient Information
MAUDE report 14610496 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K033669, K210837. One submission often covers many models, so check the product and lot details in each record.
- Z-2314-2010 · Jul 20, 2010 · TerminatedPERI-LOC (R), 3.5 MM ANTEROLATERAL DISTAL TIBIA PLATE, 10 HOLE, RIGHT - 148 MM, REF 71800710, QTY: (1), STERILE R, CE 0086, Smith & Nephew, Inc., Memphis, TN 38116, USA, EC REP:
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- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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