MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-02-04 for SONATA PUMP W/ FLEX SINGLE 1CT EN FR ES 58200 manufactured by Medela Llc.
Report Number | 1419937-2020-00006 |
MDR Report Key | 9666252 |
Report Source | CONSUMER |
Date Received | 2020-02-04 |
Date of Event | 2019-12-30 |
Date Mfgr Received | 2020-01-09 |
Device Manufacturer Date | 2019-04-04 |
Date Added to Maude | 2020-02-04 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JAN KLOIBER |
Manufacturer Street | 1101 CORPORATE DRIVE |
Manufacturer City | MCHENRY IL 60050 |
Manufacturer Country | US |
Manufacturer Postal | 60050 |
Manufacturer Phone | 8004358316 |
Manufacturer G1 | MEDELA LLC |
Manufacturer Street | 1101 CORPORATE DRIVE |
Manufacturer City | MCHENRY IL 60050 |
Manufacturer Country | US |
Manufacturer Postal Code | 60050 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SONATA PUMP W/ FLEX SINGLE 1CT EN FR ES |
Generic Name | PUMP, BREAST, POWERED |
Product Code | HGX |
Date Received | 2020-02-04 |
Returned To Mfg | 2020-01-24 |
Model Number | 58200 |
Catalog Number | 58200 |
Lot Number | 452801 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDELA LLC |
Manufacturer Address | 1101 CORPORATE DRIVE MCHENRY IL 60050 US 60050 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-04 |