Peri-Loc 71161020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010179715), received between Oct 1, 2020 and Oct 1, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Corroded” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 1, 2020Corroded; Corroded

  IT WAS REPORTED THAT ON (B)(6) JULY 10,2020 A PATIENT WAS ADMITTED TO THE HOSPITAL FOR RIGHT PATELLA FRACTURE. THE ISSUE WAS TREATED; METAL FRACTURE WAS USED TO FIX THE FRACTURE END OF THE PATELLA. ON (B)(6) 2020, A 1 CM LONG INCISION WAS SEEN IN THE FRONT OF THE RIGHT KNEE, WITH A SMALL AMOUNT OF LIGHT YELLOW LIQUID EXUDATION, AND GRADUALLY SKIN ULCERATION. ON (B)(6) 2020, AFTER THE OPERATION OF RIGHT PATELLA FRACTURE UNDER SPINAL ANESTHESIA, FOREIGN BODY REACTION, INTERNAL FIXATION REMOVAL, DEBRIDEMENT AND VSD DRAINAGE WERE PERFORMED. THE TISSUE AROUND THE END OF PERI-LOC K-WIRE 2.0MM AND STEEL WAS ERODED. THE POSTOPERATIVE CONDITION IS BETTER THAN BEFORE, AND IT IS STILL IN THE STATE OF VSD DRAINAGE.

  Patient problems: Pain; Ulcer

  MAUDE report 10617288 ↗