MLPD BASE POST WITH LOCK SCREW 7" 5875-03Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842430110238), received between Jun 9, 2020 and Jun 9, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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 18, 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.

• InjuryJun 9, 2020Patient-Device Incompatibility; Patient-Device Incompatibility

  PATIENT WAS POSITIONED ON MIZUHO BLACK WILSON FRAME FOR SPINE PROCEDURE. PROCEDURE LASTED 3 HOURS 13 MINUTES. AFTER PROCEDURE PATIENT FLIPPED BACK SUPINE. RED, BLISTERED AREAS NOTED DOWN BOTH SIDES OF PATIENT WHERE THE PATIENT WAS RESTING ON THE FOAM PADS. PADS HAD BEEN REPLACED ON THE FRAME AROUND SIX MONTHS AGO. FRAME HAS BEEN USED MANY TIMES SINCE THEN. DISPOSABLE SHEET FROM OUR CUSTOM TURNOVER KIT WAS USED TO COVER THE FRAME. SIVADENE CREAM USED TO TREAT PATIENT WOUNDS. PATIENT DISCHARGED AND WILL RECEIVE TREATMENT IN OUTPATIENT WOUND CENTER.

  Patient problems: Pressure Sore/Ulcer; Skin Irritation

  MAUDE report 10135704 ↗