Peri-Loc 71823038Recalls & reported problems
Smith & Nephew, Inc. · PERI-LOC 2.7MM SELF-TAPPING CORTEX SCREW 38MM · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010526410), received between Dec 19, 2017 and Dec 19, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
1 other recall cover devices cleared under the same FDA submission (K033669); 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
- Insufficient Device Problem Information1
Patient problems
- Erythema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 19, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THE PATIENT HAD SURGERY ON (B)(6) 2016, ORIF RIGHT CALCANEUS. THE PATIENT C/O INFECTION TO SURGICAL SITE. PHYSICAL EXAM NOTED SMALL ERYTHEMIC SEEPING WOUND TO MEDIAL ASPECT OF LEFT ANKLE. HE WAS TAKEN TO SURGERY ON (B)(6) 2017 FOR IRRIGATION AND DEBRIDEMENT OF ANKLE WITH REMOVAL OF TWO SCREWS.
Patient problems: Erythema
MAUDE report 7129873 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K033669. 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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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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