MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-26 for 20-8226V-50 HYH,CORFLO,NG-TUBE,NA,6FR,50 104716400 manufactured by Avanos Medical Inc..
Report Number | 9611594-2020-00052 |
MDR Report Key | 9882548 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-03-26 |
Date of Report | 2020-03-26 |
Date Mfgr Received | 2020-02-26 |
Date Added to Maude | 2020-03-26 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. LISA CLARK |
Manufacturer Street | 5405 WINDWARD PARKWAY |
Manufacturer City | ALPHARETTA GA 30004 |
Manufacturer Country | US |
Manufacturer Postal | 30004 |
Manufacturer Phone | 4704485444 |
Manufacturer G1 | AVENT SA DE R.L. DE C.V. (AVENT 1) |
Manufacturer Street | CIRCUITO INDUSTIAL NO.40 COLONIA OBRERA |
Manufacturer City | NOGALES, CP 84048 |
Manufacturer Country | MX |
Manufacturer Postal Code | 84048 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 20-8226V-50 HYH,CORFLO,NG-TUBE,NA,6FR,50 |
Generic Name | DH CPK NG TUBES |
Product Code | KNT |
Date Received | 2020-03-26 |
Returned To Mfg | 2020-03-06 |
Model Number | 20-8226V-50 |
Catalog Number | 104716400 |
Lot Number | 0002982982 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | AVANOS MEDICAL INC. |
Manufacturer Address | 5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-26 |