Power-PRO 2 650700000000Recalls & reported problems
Stryker Corporation · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This Stryker Power-PRO 2 ambulance stretcher. Reports mostly describe difficulty raising, lowering, or securing the cot — hard to position or remove from its mount — plus the cot tipping over or dropping unexpectedly. Of 43 reports, 1 death was reported and no injuries. Two open recalls: one started May 2023 over a base leg that can bend, causing the cot to tip or move unexpectedly; the other, from November 2022, covers damaged cables that let the cot drop faster than intended, which can scrape or bruise patients.
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
- 42
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 42 adverse event reports that list this exact device (DI 07613327504460), received between Jul 27, 2022 and Apr 22, 2026 — classified as 1 death, 41 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (13 reports).
2 FDA recall records name this device's identifier, 2 still open.
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.
Reports received per month
Recalls naming this device
- May 24, 2023Class IIOpen, Classified
Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.
Z-2130-2023 · Root cause: Process control · Recall details · FDA record ↗
- Nov 11, 2022Class IIOpen, Classified
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Z-0479-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Difficult or Delayed Positioning13
- Difficult to Remove11
- Positioning Failure9
- Device Fell4
- Device Tipped Over3
- Adverse Event Without Identified Device or Use Problem2
- Mechanical Problem2
- Electrical /Electronic Property Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions38
- Pain3
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 42 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 22, 2026Protective Measures Problem
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 INADEQUATE PATIENT RESTRAINT. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24958365 ↗MalfunctionApr 22, 2026Patient Device Interaction Problem
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 NON ERGONOMIC FEATURE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24958358 ↗MalfunctionJan 26, 2026Difficult or Delayed Positioning
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24181417 ↗MalfunctionOct 24, 2025Positioning Failure; Positioning Failure
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23383717 ↗MalfunctionOct 24, 2025Difficult to Remove; Difficult to Remove
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 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED INABILITY TO DISENGAGE THE COT FROM THE COT FASTENER. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23383711 ↗MalfunctionOct 24, 2025Difficult or Delayed Positioning; Positioning Failure; Difficult or Delayed Positioning; Positioning Failure
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23383708 ↗MalfunctionOct 24, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT NOW SUMMARIZES 5 MALFUNCTION EVENT(S), INSTEAD OF 6.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23383705 ↗DeathOct 23, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A TRAIN TRAVELING AT APPROXIMATELY EIGHTY KM PER HOUR COLLIDED WITH A STATIONARY AMBULANCE CAR. A PATIENT WAS LYING ON THE DEVICE AND PASSED AWAY AS A RESULT OF THE ACCIDENT.
Patient problems: Insufficient Information
MAUDE report 23372771 ↗MalfunctionJul 25, 2025Device Tipped Over; Device Tipped Over
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED COT TIP OR DROP (DURING LOAD/UNLOAD). NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22620736 ↗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 22608291 ↗MalfunctionJul 25, 2025Difficult to Remove; Difficult to Remove
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED INABILITY TO DISENGAGE THE COT FROM THE COT FASTENER. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22608268 ↗MalfunctionJul 25, 2025Device Fell; Device Fell
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22608071 ↗MalfunctionApr 29, 2025Difficult 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. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21925495 ↗MalfunctionApr 28, 2025Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FALSE ENGAGEMENT OF HANDLE IN THE UPRIGHT OR HORIZONTAL POSITION. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21919961 ↗MalfunctionJan 30, 2025Difficult to Remove; Difficult to Remove
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED AN INABILITY TO DISENGAGE THE COT FROM THE COT FASTENER. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277413 ↗MalfunctionJan 30, 2025Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FALSE ENGAGEMENT OF THE HANDLE IN THE UPRIGHT OR HORIZONTAL POSITION OR COT HEIGHT WHICH CANNOT BE ADJUSTED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277412 ↗MalfunctionJan 30, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning
THIS REPORT SUMMARIZES 4 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED DIFFICULTY LOADING OR UNLOADING THE COT IN THE AMBULANCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277408 ↗MalfunctionJan 30, 2025Difficult to Remove; Device Fell; Difficult to Remove; Device Fell
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED A COT DROP AND AN INABILITY TO DISENGAGE THE COT FROM THE COT FASTENER. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277407 ↗MalfunctionJan 30, 2025Device Tipped Over; Device Tipped Over
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED COT TIP. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277404 ↗MalfunctionOct 29, 2024Difficult to Remove; Difficult to Remove
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS, 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 20560680 ↗MalfunctionOct 29, 2024Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 6 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FALSE ENGAGEMENT OF HANDLE IN THE UPRIGHT OR HORIZONTAL POSITION OR COT HEIGHT CANNOT BE ADJUSTED. THERE WERE 2 EVENTS WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20559391 ↗MalfunctionOct 29, 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 20556641 ↗MalfunctionJul 29, 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 1 EVENT WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19850322 ↗MalfunctionJul 29, 2024Positioning Failure; Positioning Failure
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FOWLER CANNOT BE LOWERED OR FALSE ENGAGEMENT OF HANDLE IN THE UPRIGHT OR HORIZONTAL POSITION. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19850319 ↗MalfunctionJul 29, 2024Difficult to Remove; Difficult to Remove
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICES 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 19850294 ↗
Other STRETCHER, WHEELED devices
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- 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
- NA 0747Stryker Corporation · STRETCHER, WHEELED1 recall87 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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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