PERI-LOC 74820504Recalls & reported problems
Smith & Nephew, Inc. · 4.5MM PROXIMAL FEMUR LOCKING PLATE 4 HOLE RIGHT 144MM · 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 03596010624451), received between Apr 28, 2022 and Apr 28, 2022 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Anemia1
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
"US LEGAL" IT WAS REPORTED THAT DURING A RIGHT FEMUR REMOVAL OF HARDWARE, REVISION OF NONUNION AND IM NAILING WITH ORIF ON (B)(6) 2021, THE PATIENT SUFFERED FROM ACUTE BLOOD LOSS ANEMIA AND HYPOKALEMIA. THE PATIENT RECEIVED A BLOOD TRANSFUSION TO MAINTAIN HGB LEVELS STABLE. THE OUTCOME OF THE PATIENT IS UNKNOWN.
Patient problems: Anemia; Bruise/Contusion
MAUDE report 14243327 ↗
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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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