FDA Adverse Event Other Summary report: N

V-CATH

MDR report key: 2026229 · Received March 14, 2011

Report

Report Number
2925153-2011-00005
Event Type
Other
Date Received
March 14, 2011
Date of Event
January 25, 2011
Report Date
March 9, 2011
Manufacturer
NEO MEDICAL, INC.
Product Code
DQY
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

AS NOTED ON INTERNAL REPORT# (B)(4) FROM (B)(4) HOSP, FAXED TO NEO MEDICAL ON (B)(6) 2011 FROM MEDSPEC, INC. (DISTRIBUTOR): PICC LINE DISCONNECTED AT CATHETER SITE AND HUB, LINE WAS DC'D. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 V-CATH V-CATH 3.9FR 320CM DLL PICC DQY NEO MEDICAL, INC. 3929-2630

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention