MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-28 for AIRLIFE MISTY FINITY DIRECT CONNECT LARGE VOLUME CONTINUOUS NEBULIZER 002502 manufactured by Vyaire Medical.
Report Number | 8030673-2020-00071 |
MDR Report Key | 9639888 |
Report Source | USER FACILITY |
Date Received | 2020-01-28 |
Date of Report | 2019-12-09 |
Date of Event | 2019-12-09 |
Date Mfgr Received | 2020-02-27 |
Device Manufacturer Date | 2020-02-27 |
Date Added to Maude | 2020-01-28 |
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 | MS. MINDY FABER |
Manufacturer Street | 26125 N. RIVERWOODS BLVD. |
Manufacturer City | METTAWA IL 60045 |
Manufacturer Country | US |
Manufacturer Postal | 60045 |
Manufacturer Phone | 8727570116 |
Manufacturer G1 | PRODUCTOS UR |
Manufacturer Street | CERRADA V |
Manufacturer City | MEXICALI, 21397 |
Manufacturer Country | MX |
Manufacturer Postal Code | 21397 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AIRLIFE MISTY FINITY DIRECT CONNECT LARGE VOLUME CONTINUOUS NEBULIZER |
Generic Name | NEBULIZER (DIRECT PATIENT INTERFACE) |
Product Code | CAF |
Date Received | 2020-01-28 |
Model Number | AIRLIFE MISTY FINITY DIRECT CONNECT LARGE VOLUME C |
Catalog Number | 002502 |
Lot Number | 0004115366 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VYAIRE MEDICAL |
Manufacturer Address | 22745 SAVI RANCH PKWY YORBA LINDA CA 92887 US 92887 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-28 |