FREESTYLE BREAST PUMP - SINGLE 101034712

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-13 for FREESTYLE BREAST PUMP - SINGLE 101034712 manufactured by Medela Ag.

MAUDE Entry Details

Report Number1419937-2020-00010
MDR Report Key9707453
Date Received2020-02-13
Date of Event2020-01-22
Date Mfgr Received2020-01-22
Device Manufacturer Date2019-02-18
Date Added to Maude2020-02-13
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 AG
Manufacturer StreetLATTICHSTRASSE 4B
Manufacturer CityBAAR ZUG 6341
Manufacturer CountrySZ
Manufacturer Postal Code6341
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFREESTYLE BREAST PUMP - SINGLE
Generic NamePUMP, BREAST, POWERED
Product CodeHGX
Date Received2020-02-13
Returned To Mfg2020-02-11
Model Number101034712
Catalog Number101034712
Lot NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDELA AG
Manufacturer AddressLATTICHSTRASSE 4B BAAR ZUG 6341 SZ 6341


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-13

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