FDA Adverse Event
Injury
Summary report: N
INTROCAN SAFETY
MDR report key: 3854252
·
Received May 19, 2014
Report
- Report Number
- 9610825-2014-00192
- Event Type
- Injury
- Date Received
- May 19, 2014
- Manufacturer
- B. BRAUN MELSUNGEN AG
- Product Code
- FOZ
- PMA / PMN Number
- K982805
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN (B)(4). THE DEVICE IS CURRENTLY SHIPPING FROM (B)(4) FOR INVESTIGATION. A F/U REPORT WILL BE PROVIDED AFTER THE INSPECTION RESULTS BECOME AVAILABLE.
Description of Event or Problem · 1
REF IMP # (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 297708 | INTROCAN SAFETY | I.V. SAFETY CATHETER | FOZ | B. BRAUN MELSUNGEN AG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |