MX-PRO 6083Recalls & reported problems
Stryker Corporation · Class 2
All models of MX-PRO (2)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Stryker MX-PRO 6083 wheeled stretcher is used to move patients, including loading them into ambulances. Its reports mostly describe sharp metal edges on the frame, height settings that would not adjust or were hard to change, and stretches where the stretcher would not settle into position or position itself properly. There are 56 reports, with 1 death and 3 injuries; most reports mention no harm to the patient. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 56
- Deaths reported
- 1
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 56 adverse event reports that list this exact device (DI 07613327261585), received between Jun 12, 2018 and Apr 23, 2026 — classified as 1 death, 3 injuries, 52 malfunctions.
The most frequently reported specific device problem is “Sharp Edges” (17 reports).
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.
Reports received per month
Most reported problems
Device problems
- Sharp Edges17
- Difficult or Delayed Positioning15
- Positioning Failure13
- Device Fell6
- Device Tipped Over3
- Break2
- Device Dislodged or Dislocated2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions34
- No Patient Involvement9
- No Consequences Or Impact To Patient7
- Injury3
- Bone Fracture(s)1
- Death1
- Insufficient Information1
- Muscle/Tendon Damage1
Recent adverse event reports
The 25 most recent of 56 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Device Dislodged or Dislocated
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 COT FALSELY ENGAGES INTO FASTENER. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24967207 ↗MalfunctionJan 27, 2026Difficult or Delayed Positioning
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24189299 ↗MalfunctionJan 30, 2025Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277789 ↗MalfunctionOct 29, 2024Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20556520 ↗MalfunctionJul 26, 2024Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19843251 ↗MalfunctionJul 26, 2024Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED COT HEIGHT CANNOT BE ADJUSTED. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19840433 ↗MalfunctionApr 23, 2024Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19163129 ↗MalfunctionApr 22, 2024Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19159626 ↗MalfunctionJan 24, 2024Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18572828 ↗MalfunctionOct 25, 2023Positioning Failure; Sharp Edges; Positioning Failure; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE SHARP METAL EDGES AND FOWLER CANNOT BE LOWERED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18007342 ↗MalfunctionOct 24, 2023Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17999048 ↗MalfunctionOct 24, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17999046 ↗MalfunctionSep 8, 2023Difficult to Remove; Difficult to Remove
IT WAS REPORTED THAT THE MANUAL RELEASE WAS NOT FUNCTIONING ON THE DEVICE. IT WAS FURTHER REPORTED THAT THE PATIENT OR USER SUSTAINED AN UNSPECIFIED INJURY.
Patient problems: Insufficient Information
MAUDE report 17710722 ↗MalfunctionJul 18, 2023Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17343973 ↗MalfunctionJul 18, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULTY LOADING AND UNLOADING THE COT INTO THE AMBULANCE. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17343400 ↗MalfunctionApr 25, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULTY LOADING AND UNLOADING HE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16807286 ↗MalfunctionApr 25, 2023Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED AN INABILITY TO ADJUST THE COT HEIGHT. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT THOUGH NO ADVERSE EVENT WAS ALLEGED TO HAVE OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16807275 ↗MalfunctionApr 25, 2023Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16807274 ↗MalfunctionJan 19, 2023Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16206532 ↗MalfunctionJan 19, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED COT DISENGAGES FROM FASTENER UNEXPECTEDLY/FALSE ENGAGING INTO FASTENER. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16205068 ↗MalfunctionOct 20, 2022Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULTY LOADING/UNLOADING THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15640460 ↗MalfunctionJul 26, 2022Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULTY LOADING/UNLOADING THE COT INTO THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15106742 ↗MalfunctionJul 26, 2022Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15106736 ↗MalfunctionJul 26, 2022Positioning Failure; Sharp Edges; Positioning Failure; Sharp Edges
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT IN WHICH THE DEVICE WAS CONCURRENTLY EXPERIENCING 2 ISSUES: SHARP METAL EDGES AND THE FOWLER IS STUCK IN A RAISED POSITION. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15106601 ↗MalfunctionApr 26, 2022Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14207751 ↗
Other STRETCHER, WHEELED devices
- Power-PRO 6506Stryker Corporation · STRETCHER, WHEELED5 deaths472 reports
- Procedural stretcher P8000HHill-Rom de México, S. de R.L. de C.V. · STRETCHER, WHEELED361 reports
- Prime Series 1115Stryker Corporation · STRETCHER, WHEELED1 death251 reports
- Prime Series 1115Stryker Corporation · STRETCHER, WHEELED1 recall199 reports
- Power-PRO 2, High Configuration 650705550001Stryker Corporation · STRETCHER, WHEELED2 recalls2 deaths99 reports
- NA 1089Stryker Corporation · STRETCHER, WHEELED175 reports
- NA 5050Stryker Corporation · STRETCHER, WHEELED1 recall99 reports
- 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 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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