ProCuityRecalls & reported problems across all models

We found 17 models of ProCuity by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 368 adverse event reports in the FDA's MAUDE database, received between Jan 11, 2021 and Jul 28, 2026 — classified as 1 death, 13 injuries, 354 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (67 reports).

13 FDA recall records name at least one of these models by its device identifier, 13 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

ProCuity recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0436-2024 · Root cause: Process control · Recall details · FDA record ↗

2. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0435-2024 · Root cause: Process control · Recall details · FDA record ↗

3. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0434-2024 · Root cause: Process control · Recall details · FDA record ↗

4. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0433-2024 · Root cause: Process control · Recall details · FDA record ↗

5. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0432-2024 · Root cause: Process control · Recall details · FDA record ↗

6. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0431-2024 · Root cause: Process control · Recall details · FDA record ↗

7. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0430-2024 · Root cause: Process control · Recall details · FDA record ↗

8. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0429-2024 · Root cause: Process control · Recall details · FDA record ↗

9. Aug 30, 2023Open, Classified

   Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

   Z-0428-2024 · Root cause: Process control · Recall details · FDA record ↗

10. Aug 30, 2023Open, Classified

    Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

    Z-0427-2024 · Root cause: Process control · Recall details · FDA record ↗

11. Aug 30, 2023Open, Classified

    Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

    Z-0426-2024 · Root cause: Process control · Recall details · FDA record ↗

12. Aug 30, 2023Open, Classified

    Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

    Z-0425-2024 · Root cause: Process control · Recall details · FDA record ↗

13. Aug 30, 2023Open, Classified

    Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

    Z-0424-2024 · Root cause: Process control · Recall details · FDA record ↗

Most reported ProCuity problems

ProCuity models

17 models, most reported first. Each model has its own page with its reports, recalls and device details.

• ProCuity 300900000000

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall111 reports
• ProCuity 3009PX-LEX-400

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall1 death67 reports
• ProCuity 3009PX-ZMX-600

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall63 reports
• ProCuity 3009PX-LEX-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall57 reports
• ProCuity 3009PX-LE-400

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall12 reports
• ProCuity 3009PX-ZM-600

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall9 reports
• ProCuity 3009PX-ZX-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall6 reports
• ProCuity 3009PX-LE-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall5 reports
• ProCuity 3009PX-L-200

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall4 reports
• ProCuity 3009PX-L-100

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall2 reports
• ProCuity 3009PX-Z-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall1 report
• ProCuity 3009PX-ZMX-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall1 report
• ProCuity 3009PX-ZM-450

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 recall0 reports
• ProCuity 3009PX-ZX-400

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  23 reports
• ProCuity 3009PX-Z-400

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  3 reports
• ProCuity 3009PX-ZMX-400

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  3 reports
• ProCuity 3009PX-ZM-500

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 report

Recent ProCuity adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionJul 28, 2026Patient Device Interaction Problem

  Patient problems: Physical Entrapment

  MAUDE report 50062278 ↗
• MalfunctionJul 28, 2026No Audible Alarm

  Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 50060446 ↗
• MalfunctionJul 27, 2026Device Fell

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50045834 ↗
• InjuryJul 21, 2026No Audible Alarm

  IT WAS ALLEGED THAT A PATIENT FELL OUT OF BED AND THE BED ALARM DID NOT ALERT. IT WAS REPORTED THAT THE PATIENT SUSTAINED A PELVIC FRACTURE THAT WAS TREATED WITH SURGERY.

  Patient problems: Bone Fracture(s)

  MAUDE report 25895807 ↗
• 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 2 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FOWLER UNEXPECTED DROP/COLLAPSE OR LITTER/LIFT UNEXPECTED DROP/COLLAPSE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966928 ↗
• MalfunctionApr 23, 2026No Audible Alarm

  THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. EVENTS OCCURRED BETWEEN (B)(6) ¿ (B)(6) 2026. THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED CLINICIAN NOT ALERTED/AWARE OF POSSIBLE PATIENT FALL CONDITION. THERE WERE 2 EVENTS WITH PATIENT INVOLVEMENT; THE PATIENTS EXPERIENCED A FALL. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966927 ↗
• 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 6 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FOWLER UNEXPECTED DROP/COLLAPSE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966912 ↗
• MalfunctionApr 23, 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 TRIPPING HAZARD; UNEXPECTED PERIMETER. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; THE PATIENT EXPERIENCED A FALL. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: Fall

  MAUDE report 24966910 ↗
• MalfunctionApr 23, 2026No Audible Alarm

  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 2 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES, EXPERIENCED CLINICIAN NOT ALERTED/AWARE OF POSSIBLE PATIENT FALL CONDITION. THERE WAS 1 EVENT WITH PATIENT INVOLVEMENT; THE PATIENT EXPERIENCED A FALL. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966660 ↗
• 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 3 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED FOWLER UNEXPECTED DROP/COLLAPSE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966658 ↗
• DeathApr 9, 2026No Audible Alarm

  IT WAS REPORTED THAT THE BED EXIT FAILED TO ALARM WHEN THE PATIENT GOT OUT OF THE BED. THE PATIENT WAS FOUND BY STAFF ON THE FLOOR IN A STATE OF CARDIAC ARREST. THE PATIENT REPORTEDLY PASSED AWAY.

  Patient problems: Cardiac Arrest; Fall

  MAUDE report 24832929 ↗
• MalfunctionJan 27, 2026Device Fell

  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 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED FOWLER UNEXPECTED DROP/COLLAPSE. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24189132 ↗
• MalfunctionJan 27, 2026Unintended System Motion

  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 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED UNINTENDED DIRECTION OF THE ZOOM; UNINTENDED MOTION. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24189128 ↗
• MalfunctionJan 27, 2026Sharp Edges

  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 1 MALFUNCTION EVENT(S), WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE SHARP METAL EDGES. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24189127 ↗
• MalfunctionJan 27, 2026No Audible Alarm

  NO NEW INFORMATION.

  Patient problems: Abrasion; Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24189122 ↗

Other Stryker Corporation products

• RemB7 models · 3,073 reports
• Prime Series21 models · 1,548 reports · 2 recalls
• TARGET114 models · 1,077 reports
• Spetzler-Malis20 models · 7 reports · 19 recalls
• SYNCHRO 28 models · 313 reports · 9 recalls
• Neptune E-SEP19 models · 412 reports · 7 recalls
• StrykeFlow4 models · 552 reports · 4 recalls
• InTouch5 models · 666 reports · 1 recall