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