STERRAD VELOCITY? BI 43210

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 2018-06-14 for STERRAD VELOCITY? BI 43210 manufactured by Advanced Sterilization Products.

Event Text Entries

[111168627] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[111168628] A customer reported a positive result with a sterrad? Velocity? Biological indicator (bi) after a completed sterrad? 100s cycle. The affected load was released and used on a patient. There was no report of infection, injury or harm to patient(s) associated with this issue. Although there is no report of patient injury or harm and no prior incidents have resulted in serious injury, advanced sterilization products (asp) has determined in this situation sterility cannot be assured. Therefore, as a matter of policy asp had decided to report all incidents of positive sterrad? Velocity? Biological indicators when the load has been released prior to reprocessing.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2084725-2018-00634
MDR Report Key7601176
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-06-14
Date of Report2018-05-21
Date of Event2018-05-07
Date Mfgr Received2018-11-15
Device Manufacturer Date2018-01-08
Date Added to Maude2018-06-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. GABRIEL ALFAGEME
Manufacturer Street33 TECHNOLOGY DRIVE
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer G1ADVANCED STERILIZATION PRODUCTS
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 VELOCITY? BI
Generic NameINDICATOR, BIOLOGICAL
Product CodeFRC
Date Received2018-06-14
Returned To Mfg2018-08-20
Catalog Number43210
Lot Number0081802
Device Expiration Date2018-10-08
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerADVANCED STERILIZATION PRODUCTS
Manufacturer Address33 TECHNOLOGY DRIVE IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.