MCKESSON S1667G

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-17 for MCKESSON S1667G manufactured by Surgical Specialties Mexico.

MAUDE Entry Details

Report Number3010692967-2019-00022
MDR Report Key8798293
Date Received2019-07-17
Date of Report2019-07-17
Date of Event2019-06-18
Date Facility Aware2019-06-18
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2005-01-14
Device Manufacturer Date2015-09-01
Date Added to Maude2019-07-17
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 ContactMS. KELLY KNAPPENBERGER
Manufacturer Street1100 BERKSHIRE BLVD. STE 308
Manufacturer CityREADING PA 19608
Manufacturer CountryUS
Manufacturer Postal19608
Manufacturer G1SURGICAL SPECIALTIES CORPORATION
Manufacturer StreetCORREDOR TIJUANA-ROSARITO 2000 #24702B EJIDO FRANCISCO VILLA
Manufacturer CityTIJUANA 22235
Manufacturer CountryMX
Manufacturer Postal Code22235
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMCKESSON
Generic NameMCK DSM18 4-0 BMN 18"/46CM
Product CodeGAB
Date Received2019-07-17
Model NumberS1667G
Catalog NumberS1667G
Lot NumberMANA880
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age4 YR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSURGICAL SPECIALTIES MEXICO
Manufacturer AddressCORREDOR TIJUANA ROSARITO 2000 24702-B EJIDO FRANCISCO VILLA TIJUANA 22235 MX 22235


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-17

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