inforMED
MalfunctionFLE

AMSCO

Received Jul 25, 2024

Report 3005899764-2024-00034 · MDR key 19828618

Device

Generic name

Sterilizer

Catalog number

EF1301142

Product problems

  • No Apparent Adverse Event
  • No Apparent Adverse Event

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

THE FEBRUARY 2024 PREVENTIVE MAINTENANCE SERVICE REQUEST TICKETS FOR THE SUBJECT AMSCO 600 STEAM STERILIZERS ((B)(4)) WERE OPENED ON 1/30/2024. THE STERIS SERVICE TECHNICIAN WAS AWARE OF THE BACKORDERED PARTS TO COMPLETE THE PREVENTIVE MAINTENANCE (PM) ACTIVITY AND WAS UNABLE TO COMPLETE THE PMS UNTIL ALL COMPONENTS WERE AVAILABLE. ALL PM ACTIVITIES FOR THE UNITS WERE COMPLETED IN MARCH 2024 AND THE AMSCO 600 STEAM STERILIZERS WERE RETURNED TO SERVICE. NO FURTHER SERVICE ACTIVITIES HAVE BEEN REQUESTED BY THE USER FACILITY. THE USER FACILITY PROCEEDED TO FILE MEDWATCH MW5155875, MW5155876 AND MW5155877 REPORTS WHICH STERIS RECEIVED ON JUNE 28, 2024. THE AMSCO 600 STEAM STERILIZERS SUBJECT OF THE REPORTED EVENT WERE MANUFACTURED IN 2021. THE USER FACILITY PURCHASED INSTALLATION OF THE AMSCO 600 STEAM STERILIZERS IN 2023. THE INSTALLATION OF THE UNITS WERE COMPLETED BY STERIS IN SEPTEMBER 2023. STERIS EVALUATED THE REPORTED EVENT AND DETERMINED IT DOES NOT MEET OUR REPORTING CRITERIA UNDER 21 CFR PART 803. IT SHOULD BE NOTED THAT STERIS IS SUBMITTING A MEDICAL DEVICE REPORT (MDR) SOLELY DUE TO THE RECEIPT OF THE USER FACILITY MEDWATCH REPORT WHICH IS IN ACCORDANCE WITH OUR PROCEDURES AND POLICIES. NO ADDITIONAL ISSUES HAVE BEEN REPORTED.

Description of Event or Problem

THE USER FACILITY REPORTED VIA MEDWATCH REPORTS MW5155875, MW5155876 AND MW5155877 THAT "PMS OF 3 STERILIZERS WERE CLOSED OUTSIDE THE MONTH +/- 10 DAY WINDOW FOR COMPLETING SCHEDULED PLANNED MAINTENANCE. THIS WAS DUE TO THE CONTRACTED OEMS INABILITY TO PRODUCE THE PM KITS NEEDED FOR THE EQUIPMENT DUE FOR PM."