SONATA DELUXE SINGLE PACK 58200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-02-17 for SONATA DELUXE SINGLE PACK 58200 manufactured by Medela Llc.

MAUDE Entry Details

Report Number1419937-2020-00012
MDR Report Key9717298
Report SourceCONSUMER
Date Received2020-02-17
Date of Event2020-01-28
Date Mfgr Received2020-02-03
Device Manufacturer Date2019-05-08
Date Added to Maude2020-02-17
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 ContactJAN KLOIBER
Manufacturer Street1101 CORPORATE DRIVE
Manufacturer CityMCHENRY, IL
Manufacturer CountryUS
Manufacturer Phone4358316
Manufacturer G1MEDELA LLC
Manufacturer Street1101 CORPORATE DRIVE
Manufacturer CityMCHENRY, IL
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSONATA DELUXE SINGLE PACK
Generic NamePUMP, BREAST, POWERED
Product CodeHGX
Date Received2020-02-17
Model Number58200
Catalog Number58200
Lot Number453812
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMEDELA LLC
Manufacturer Address1101 CORPORATE DRIVE MCHENRY, IL US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-17

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