Performance-LOAD 6392 (REF 6392-000-004)Recalls & reported problems
Stryker Corporation · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327282610), received between Oct 30, 2023 and Apr 23, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Device Fell” (4 reports).
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.
Reports received per month
Recalls naming this device
- 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
Device problems
- Device Fell4
- Insufficient Cooling1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Insufficient Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Device Fell
THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. EVENTS OCCURRED BETWEEN JANUARY 1- MARCH 31, 2026. THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FASTENER NO LONGER FACILITATES PROPER COT OPERATIONS DURING LOADING/UNLOADING. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24967392 ↗MalfunctionApr 28, 2025Device Fell; Device Fell
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FASTENER NO LONGER FACILITATES PROPER COT OPERATIONS DURING LOADING/UNLOADING. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21921709 ↗MalfunctionOct 29, 2024Device Fell; Device Fell
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FASTENER NO LONGER FACILITATES PROPER COT OPERATIONS DURING LOADING/UNLOADING. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20556610 ↗MalfunctionApr 10, 2024Device Fell; Device Fell
IT WAS REPORTED THAT DAMAGED COMPONENTS ON THE PERFORMANCE LOAD CAUSED THE COT TO TIP DURING UNLOADING (FASTENER NO LONGER FACILITATES PROPER COT OPERATIONS DURING LOADING/UNLOADING). THERE WAS A PATIENT ON THE COT AT THE TIME AND THEY WERE TRANSPORTED TO HOSPITAL TO BE EVALUATED FOR NON-SPECIFIED INJURIES. NO ADVERSE CONSEQUENCE WAS ALLEGED TO HAVE OCCURRED TO THE STAFF UNLOADING THE COT AT THE TIME OF THE INCIDENT.
Patient problems: Insufficient Information
MAUDE report 19082317 ↗MalfunctionOct 30, 2023Insufficient Cooling; Insufficient Cooling
IT WAS REPORTED THAT THE PATIENT WAS NOT COOLING. THE PATIENT TEMPERATURE IS 39 °C WITH A TARGET TEMPERATURE OF 33 °C, WATER TEMPERATURE IS 33 °C SET TO MANUAL MODE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18031126 ↗
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- Prime Series 1115Stryker Corporation · STRETCHER, WHEELED1 recall199 reports
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- Power-PRO 2 650700000000Stryker Corporation · STRETCHER, WHEELED2 recalls1 death42 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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