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 |