FDA Adverse Event
Other
Summary report: N
NEOMEDICAL POWER-V PICC
MDR report key: 1741503
·
Received June 28, 2010
Report
- Report Number
- 2925153-2010-00010
- Event Type
- Other
- Date Received
- June 28, 2010
- Report Date
- June 25, 2010
- Manufacturer
- NEOMEDICAL
- Product Code
- DQY
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- 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 INFO PROVIDED WITH THE REPORT TO DATE IS SKETCHY. NO PRODUCT NUMBER OR LOT NUMBER(S) HAS BEEN PROVIDED. ADDITIONAL INFO 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). ADDITIONAL CATALOG # 4 FR PICC; OTHER # 4 FR.
Description of Event or Problem · 1
BASED ON THE REPORT INFO, SUBMITTED TO (B)(4) ON (B)(6) 2010, CUSTOMER COMPLAINED THAT THERE WAS DIFFICULTY REMOVING STYLET. NO OTHER INFO 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 POWER-V PICC | V-CATH POWER-V PICC | DQY | NEOMEDICAL |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Required Intervention |