MALYUGIN RING SYSTEM 7.0MM MAL-0002-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-19 for MALYUGIN RING SYSTEM 7.0MM MAL-0002-1 manufactured by Microsurgical Technology, Inc..

Event Text Entries

[184072713] Opened malyugin ring to sterile field; scrub tech handed instrument to surgeon; surgeon advanced instrument and noticed it was bent made contact with patient; removed instrument and another malyugin ring opened to sterile field to use on patient. Manufacturer response for malyugin ring, malyugin ring (per site reporter). Pending.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9853141
MDR Report Key9853141
Date Received2020-03-19
Date of Report2020-02-04
Date of Event2020-01-15
Report Date2020-02-04
Date Reported to FDA2020-02-04
Date Reported to Mfgr2020-03-19
Date Added to Maude2020-03-19
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMALYUGIN RING SYSTEM 7.0MM
Generic NameCLIP, IRIS RETRACTOR
Product CodeHOC
Date Received2020-03-19
Returned To Mfg2020-01-28
Model NumberMAL-0002-1
Catalog NumberMAL-0002-1
Lot Number115311
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age1 DA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMICROSURGICAL TECHNOLOGY, INC.
Manufacturer Address8415 154TH AVE., N.E. REDMOND WA 98052 US 98052


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-19

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