Peri-Loc 71867066Recalls & reported problems
Smith & Nephew, Inc. · PERI-LOC 4.5MM T25 TITANIUM LOCKING SCREW 66MM SELF-TAPPING · Class 2
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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010641694), received between Jun 29, 2021 and Jun 29, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Connection Problem” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K083032, 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
- Connection Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 29, 2021Connection Problem; Connection Problem
IT WAS REPORTED THAT, DURING A TRAUMA SURGERY WHILE THE INSTRUMENT WAS INSIDE OF THE PATIENT, THE SCREW WAS NOT LOCKED AND PENETRATED THE HOLE ON THE PLATE. THE PERI-LOC 4.5MM TI L-D FEM PL 8H L 193MM, PERI-LOC 4.5MM T25 TI LCK SCR 66MM S-T, TWO (2) PERI-LOC 4.5MM T25 TI LCK SCR 64MM S-T AND PERI-LOC 4.5MM T25 TI LCK SCR 58MM S-T; IT WAS UNKNOWN IF THE PLATE OR WHICH SCREWS REPORTED WERE DEFECTIVE. THE PROCEDURE WAS SUCCESSFULLY COMPLETED PUTTING BACK AND ROTATING IN AN OPPOSITE DIRECTION WITHOUT DELAY USING THE SAME DEVICE. PATIENT WAS NOT HARMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12082287 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083032, K210837. One submission often covers many models, so check the product and lot details in each record.
- Z-0373-2016 · Oct 20, 2015 · TerminatedSmith & Nephew PERI-LOC VOLAR DISTAL RADIUS PLATE STANDARD 3 HOLE SHORT, RIGHT - 62 MM, STERILE R, Rx only, REF Numbers: 71863114 Bone fixation plate
- Z-0372-2016 · Oct 20, 2015 · TerminatedSmith & Nephew PERI-LOC VOLAR DISTAL RADIUS PLATE STANDARD 3 HOLE SHORT, LEFT - 62 MM, STERILE R, Rx only, REF Numbers: 71863110 Bone fixation plate
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- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- 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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