MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-11 for CAREFUSION CIRCUIT AND BREATHING A4UX2044 manufactured by Carefusion / Vyaire Medical, Inc..
Report Number | MW5088045 |
MDR Report Key | 8785263 |
Date Received | 2019-07-11 |
Date of Report | 2019-07-09 |
Date of Event | 2019-07-08 |
Date Added to Maude | 2019-07-12 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | CAREFUSION CIRCUIT AND BREATHING |
Generic Name | CIRCUIT, BREATHING (W CONNECTOR, ADAPTER Y PIECE |
Product Code | CAI |
Date Received | 2019-07-11 |
Model Number | A4UX2044 |
Lot Number | 0004094921 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CAREFUSION / VYAIRE MEDICAL, INC. |
Manufacturer Address | YORBA LINDA CA 10341 US 10341 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-11 |