FDA Adverse Event Malfunction Summary report: N

CARDINAL HEALTH

MDR report key: 17360684 · Received July 20, 2023

Report

Report Number
17360684
Event Type
Malfunction
Date Received
July 20, 2023
Date of Event
June 19, 2023
Report Date
June 29, 2023
Manufacturer
CARDINAL HEALTH 200, LLC
Product Code
PKF
Product Problem
Yes
Report Source
User Facility report
Reporter Location
ME
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

FROM STAFF: SPONGES FROM A PACK FOUND TO HAVE DEBRIS/BUG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
40214 CARDINAL HEALTH D AND C TRAY PKF CARDINAL HEALTH 200, LLC SMA13DCEMP 037744

Patients

Seq Age Sex Outcome Treatment
1 Unknown