Performance-LOAD 6392 (REF 6392-000-001)Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327282542), received between Apr 6, 2018 and Jul 27, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 FDA recall record name this device's identifier.

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Nov 8, 2016Terminated

   Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot Fasteners due to complaints that fastening system may not have been securely fastened or had an inability to fasten into the Performance-LOAD and bounced back during loading which could cause injury to consumers.

   Z-0739-2017 · Root cause: Under Investigation by firm · FDA record ↗

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 27, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DISENGAGEMENT OF THE FASTENER. THERE WAS PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12233828 ↗
• MalfunctionApr 26, 2019Device Fell; Device Fell

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THERE WAS A COT DROP EVENT. THERE WAS PATIENT INVOLVEMENT, HOWEVER THERE WERE NO CONSEQUENCES OR IMPACTS TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8554568 ↗
• MalfunctionOct 24, 2018Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE WHILE UNLOADING A PATIENT A MEDIC GOT HIS HAND PINCHED WHEN TRYING TO REACH UNDER THE COT. IT WAS REPORTED THAT THE MEDIC WENT TO THE EMERGENCY ROOM.

  Patient problems: Injury

  MAUDE report 8000296 ↗
• MalfunctionApr 6, 2018Fire

  IT WAS REPORTED THAT THE COT FASTENING SYSTEM AND THE ASSOCIATED VEHICLE THE COT FASTENING SYSTEM WAS INSTALLED IN CAUGHT ON FIRE. IT WAS ALLEGED BY THE CUSTOMER THAT THE INSTALLATION OF THE PRODUCT COULD HAVE CAUSED OR CONTRIBUTED TO THE EVENT.

  Patient problems: No Information

  MAUDE report 7402331 ↗