MCKESSON MEDI-PAK 16-9706

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-11-29 for MCKESSON MEDI-PAK 16-9706 manufactured by Mckesson Medical-surgical.

MAUDE Entry Details

Report Number9391800
MDR Report Key9391800
Date Received2019-11-29
Date of Report2019-11-19
Date of Event2019-02-26
Report Date2019-11-19
Date Reported to FDA2019-11-19
Date Reported to Mfgr2019-11-29
Date Added to Maude2019-11-29
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 NameMCKESSON MEDI-PAK
Generic NameINSTANT HOT COMPRESS
Product CodeIMD
Date Received2019-11-29
Catalog Number16-9706
Lot NumberCITH10-01
Device AvailabilityN
Device Age1 DA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMCKESSON MEDICAL-SURGICAL
Manufacturer Address9954 MAYLAND DRIVE, SUITE 4000 MCKESSON CORPORATION RICHMOND VA 23233 US 23233


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-29

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