Peri-Loc 71823402Recalls & reported problems
Smith & Nephew, Inc. · PERI-LOC SUPERIOR MEDIAL CLAVICLE LOCKING PLATE 10 HOLE L 121MM · 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 00885556042014), received between May 4, 2022 and May 4, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
Patient problems
- Failure of Implant1
- Nonunion/Delayed-union Bone Fracture1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 4, 2022Break; Break
IT WAS REPORTED THAT THE PATIENT UNDERWENT SURGERY ON (B)(6) 2021 FOR A CLAVICLE FRACTURE. ON (B)(6) 2022 AT NIGHT, WHILE SLEEPING, HE FELT A CLICK AND PAIN IN THE LEFT CLAVICLE, HE WENT TO THE CONSULTATION DUE TO PAIN AND, UNDER CONFIRMATION WITH X-RAYS, THERE WAS FRACTURE ON THE SUP MED CLAV LK PL 10H L 121MM. THE PATIENT WAS RE-OPERATED ON (B)(6) 2022 TO EXTRACT BROKEN MATERIAL AND NEW OSTEOSYNTHESIS WITH A COMPETITOR DEVICE. THE PATIENT'S CURRENT STATUS IS STABLE.
Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture; Pain
MAUDE report 14282797 ↗
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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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