FDA Adverse Event Malfunction Summary report: N

FREESTYLE FLEX BREAST PUMP EN FR ES

MDR report key: 10392099 · Received August 11, 2020

Report

Report Number
1419937-2020-00082
Event Type
Malfunction
Date Received
August 11, 2020
Date of Event
July 29, 2020
Manufacturer
MEDELA AG
Product Code
HGX
UDI-DI
00020451379807
PMA / PMN Number
K191653
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER WAS SENT A REPLACEMENT PUMP AND RETURN OF HER ORIGINAL PUMP WAS REQUESTED FOR TESTING/EVALUATION. THIS ISSUE IS CURRENTLY UNDER INVESTIGATION BY MEDELA AG, THE LEGAL MANUFACTURER IN (B)(4).

Description of Event or Problem · 1

ON (B)(6) 2020, THE CUSTOMER ALLEGED TO MEDELA LLC THAT HER FREESTYLE FLEX PUMP AND POWER CORD MELTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
858727 FREESTYLE FLEX BREAST PUMP EN FR ES PUMP, BREAST, POWERED HGX MEDELA AG 101037980 160193 00020451379807

Patients

Seq Age Sex Outcome Treatment
1