FDA Adverse Event
Other
Summary report: N
NEOMEDICAL V-CATH PICC
MDR report key: 1730148
·
Received June 11, 2010
Report
- Report Number
- 2925153-2010-00007
- Event Type
- Other
- Date Received
- June 11, 2010
- Report Date
- June 11, 2010
- Manufacturer
- NEOMEDICAL
- Product Code
- DQY
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- EC
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT WAS ASSESSED AND DETERMINED TO BE A MDR REPORT BASED ON OUR MDR REPORTING CRITERIA. THE INFORMATION PROVIDED WITH THE REPORT IS SKETCHY. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT HAS NOT BEEN RECEIVED. AN EXAMINATION OF THE DEVICE(S) HAS NOT BEEN CARRIED OUT AS THE USED ITEM(S) WAS NOT RETURNED TO (B)(4).
Description of Event or Problem · 1
BASED ON THE REPORT INFORMATION, SUBMITTED TO (B)(4) ON (B)(6) 2010, PICCS LEAKED DURING USE. THE PRODUCT IS (B)(4). NO OTHER INFORMATION HAS BEEN MADE AVAILABLE. THE USED PRODUCTS / SAMPLES WERE NOT RETURNED TO (B)(4). (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NEOMEDICAL V-CATH PICC | V-CATH 2 FR PICC | DQY | NEOMEDICAL | 355-72 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Required Intervention |