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MX-PRO 6082Recalls & reported problems

Stryker Corporation · Class 2

Quick summary

This Stryker wheeled stretcher has 89 adverse event reports, including 81 malfunctions, mentioning 1 death and 7 injuries; reports describe positioning difficulty, falls or tipping, and sharp edges. There are no recalls for this device. Reports fell from 6 in the previous 12 months to 2 in the most recent 12 months.

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
89
Deaths reported
1
Injuries reported
7
Recalls naming it
0

Summary

The FDA's MAUDE database contains 89 adverse event reports that list this exact device (DI 07613327261547), received between Feb 23, 2018 and Apr 23, 2026 — classified as 1 death, 7 injuries, 81 malfunctions.

The most frequently reported specific device problem is “Difficult or Delayed Positioning” (31 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 3 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 2 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 2 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 2 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 2 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Difficult or Delayed Positioning31
  • Positioning Failure17
  • Device Fell13
  • Device Tipped Over12
  • Sharp Edges5
  • Device Slipped3
  • Protective Measures Problem3
  • Improper or Incorrect Procedure or Method2

Patient problems

  • No Clinical Signs, Symptoms or Conditions48
  • No Patient Involvement16
  • No Consequences Or Impact To Patient11
  • Pain6
  • Laceration(s)4
  • Fall3
  • Muscle/Tendon Damage2
  • Bruise/Contusion1

Recent adverse event reports

The 25 most recent of 89 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 23, 2026Difficult or Delayed Positioning

    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 DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24966944 ↗
  • MalfunctionJan 27, 2026Difficult or Delayed Positioning

    THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. EVENTS OCCURRED BETWEEN OCTOBER 1-DECEMBER 31, 2025. THIS REPORT SUMMARIZES 3 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24189146 ↗
  • MalfunctionOct 27, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. EVENTS OCCURRED BETWEEN JULY 1-SEPTEMBER 30, 2025. THIS REPORT SUMMARIZES 4 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23393624 ↗
  • MalfunctionJul 25, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22608969 ↗
  • MalfunctionApr 29, 2025Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED COT HEIGHT CANNOT BE ADJUSTED. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21925778 ↗
  • MalfunctionApr 28, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 9 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED DIFFICULT TO LOAD/UNLOAD THE COT IN THE AMBULANCE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21922042 ↗
  • MalfunctionJan 28, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 3 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED DIFFICULTY LOADING AND UNLOADING THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21255285 ↗
  • MalfunctionJan 28, 2025Device Fell; Device Fell

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED A COT DROP. ALLEGEDLY A PATIENT SUSTAINED A MINOR INJURY DUE TO LACERATIONS.

    Patient problems: Laceration(s)

    MAUDE report 21255273 ↗
  • MalfunctionJul 26, 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 19840102 ↗
  • MalfunctionJul 24, 2024Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED COT HEIGHT CANNOT BE ADJUSTED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19818737 ↗
  • MalfunctionApr 23, 2024Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 3 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 19163271 ↗
  • MalfunctionApr 23, 2024Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED COT HEIGHT CANNOT BE ADJUSTED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19162959 ↗
  • MalfunctionJan 24, 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 18573175 ↗
  • MalfunctionJan 24, 2024Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 4 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 18572874 ↗
  • MalfunctionJan 24, 2024Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FOWLER CANNOT BE LOWERED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18572827 ↗
  • MalfunctionOct 25, 2023Difficult 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 18007336 ↗
  • MalfunctionOct 24, 2023Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED COT HEIGHT CANNOT BE ADJUSTED OR FOWLER CANNOT BE LOWERED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17999043 ↗
  • MalfunctionJul 18, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED DIFFICULTY LOADING AND UNLOADING THE COT INTO THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17343393 ↗
  • MalfunctionJul 18, 2023Sharp 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 17343391 ↗
  • MalfunctionApr 25, 2023Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FOWLER - CANNOT BE RAISED; STUCK IN LOWER THAN DESIRED POSITION. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16807074 ↗
  • MalfunctionApr 25, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning

    THIS REPORT SUMMARIZES 4 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 16807066 ↗
  • 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 16806890 ↗
  • MalfunctionJan 20, 2023Difficult to Remove; Difficult to Remove

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED INABILITY TO DISENGAGE THE COT FROM THE COT FASTENER. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16213946 ↗
  • MalfunctionJan 19, 2023Difficult 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 16210529 ↗
  • MalfunctionOct 24, 2022Positioning Failure; Positioning Failure

    THIS REPORT SUMMARIZES 5 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICE HEIGHT COULD NOT BE ADJUSTED OR THAT THE FOWLER WAS STUCK ELEVATED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15662694 ↗

Other STRETCHER, WHEELED devices

All STRETCHER, WHEELED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.