STERRAD? 100NX STERILIZER ALLCLEAR 1-DR DUO 10104007

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-10 for STERRAD? 100NX STERILIZER ALLCLEAR 1-DR DUO 10104007 manufactured by Advanced Sterilization Products.

Event Text Entries

[178966231] (b)(4). A field service engineer was dispatched to the customer site. The adapter converter, catalytic converter, oil mist filter, and vacuum pump oil were replaced to resolve the smoke/haze issue. Unit meets specifications and was returned to service. Asp complaint ref #: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[178966232] A customer reported an event of an odorless vapor/smoke emitting from the sterrad? 100nx sterilizer and one healthcare worker (hcw) experienced irritation, burning, and itchiness in the eye. Upon follow-up, the hcw noted he took his contacts off to rinse and flush his eyes, and the reaction lasted 4 hours. The hcw also had a? Light headache? Which lasted 1 hour. However, the hcw did not receive medical attention/treatment for his symptoms. The customer was advised to clear the facility and shut down the unit until serviced. An asp field service engineer was dispatched to assess the unit onsite. The injuries reported were not considered serious as the symptoms resolved on their own without any medical treatment. However, this event is being reported as a malfunction subsequent to a serious injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2084725-2019-00010
MDR Report Key9578279
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-10
Date of Report2020-01-10
Date of Event2019-12-19
Date Mfgr Received2019-12-20
Device Manufacturer Date2000-01-01
Date Added to Maude2020-01-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. GABRIELA MCLELLAN
Manufacturer Street33 TECHNOLOGY DRIVE
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9494536386
Manufacturer G1ASP IRVINE MFG
Manufacturer Street33 TECHNOLOGY DRIVE
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal Code92618
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTERRAD? 100NX STERILIZER ALLCLEAR 1-DR DUO
Generic NameSTERRAD EQUIPMENT
Product CodeMLR
Date Received2020-01-10
Catalog Number10104007
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerADVANCED STERILIZATION PRODUCTS
Manufacturer Address33 TECHNOLOGY DRIVE IRVINE CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-10

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