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AMSCO 7052HP (REF FH18042)Recalls & reported problems

Corporation Steris Canada · The AMSCO 7052HP Washer-Disinfector with Steam Heat delivers a validated and cleared process for cleaning reusable da Vinci EndoWrist X/Xi, S/Si, and Single-Site instruments and staplers. · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995176587), received between Jun 15, 2023 and Apr 9, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Fire” (1 report).

1 FDA recall record name this device's identifier, 1 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Nov 19, 2025Open, Classified

    Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).

    Z-0909-2026 · Root cause: Process control · FDA record ↗

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Fire1
  • Leak/Splash1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Bruise/Contusion1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 9, 2026Adverse Event Without Identified Device or Use Problem

    THE USER FACILITY REPORTED THAT WHILE REMOVING INSTRUMENTS FROM AN AMSCO 7052 HP WASHER/DISINFECTOR, THE WASHER DOOR CONTACTED ON AN EMPLOYEE'S FOREARM, RESULTING IN A BRUISE. THE DOOR RETRACTED AFTER CONTACTING THE EMPLOYEE'S FOREARM, AND THE SAFETY BAR FUNCTIONED AS DESIGNED. MEDICAL TREATMENT WAS SOUGHT; HOWEVER, IT IS UNKNOWN WHAT MEDICAL TREATMENT WAS ADMINISTERED.

    Patient problems: Bruise/Contusion

    MAUDE report 24835638 ↗
  • MalfunctionFeb 20, 2026Leak/Splash

    THE USER FACILITY REPORTED AN EMPLOYEE "SLIPPED BUT DID NOT FALL" ON LUBRICANT LEAKING FROM THEIR AMSCO 7052HP WASHER/DISINFECTOR. THE LEAK WAS QUICKLY CONTAINED AND THE EMPLOYEE CONTINUED WORKING. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24402863 ↗
  • MalfunctionJun 15, 2023Fire; Fire

    THE USER FACILITY REPORTED THAT THEIR AMSCO 7052 HP WASHER/DISINFECTOR CAUGHT FIRE. THE FIRE WAS EXTINGUISHED. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17134473 ↗

Other Disinfector, medical devices devices

All Disinfector, medical devices devices →

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