FDA Adverse Event
Injury
Summary report: N
B. BRAUN MEDICAL INC.
MDR report key: 2192932
·
Received February 1, 2008
Report
- Report Number
- 2192932
- Event Type
- Injury
- Date Received
- February 1, 2008
- Date of Event
- January 7, 2008
- Report Date
- February 1, 2008
- Manufacturer
- B. BRAUN MED. INC.
- Product Code
- NGT
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- CA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
ON (B)(6) 2008, PATIENT WAS ADMITTED TO THE HOSPITAL FOR WEAKNESS, FATIGUE AND FLANK PAIN. BLOOD CULTURES ON (B)(6) 2008 RETURNED POSITIVE FOR SERRATIA MARCESCENS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | B. BRAUN MEDICAL INC. | HEPARIN AND NORMAL SALINE PRE-FILLED FLUSHES | NGT | B. BRAUN MED. INC. | NDC# 64054-1003-02 | ||
| 2 | B. BRAUN MEDICAL INC. | HEPARIN AND NORMAL SALINE PRE-FILLED FLUSHES | NZW | B. BRAUN MED. INC. | NDC# 6405-0910-2 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 82 YR | Hospitalization |