FDA Adverse Event No answer provided Summary report: N

BILATERAL KNEE PACK

MDR report key: 16537076 · Received March 14, 2023

Report

Report Number
16537076
Event Type
No answer provided
Date Received
March 14, 2023
Date of Event
January 24, 2023
Report Date
February 27, 2023
Manufacturer
CARDINAL HEALTH 200, LLC
Product Code
OJH
Report Source
User Facility report
Reporter Location
CT
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

BILATERAL KNEE PACK CONTENTS LISTED AS CONTAINING 4 PACKS OF X-RAY LAP SPONGES. WHEN PACK OPENED, ONLY 3 PACKS OF X-RAY LAP SPONGES PRESENT. ISSUE FOUND AND RESOLVED PRIOR TO PATIENT ENTERING OR. CHARGE RN AND MATERIALS AWARE. NO HARM TO PATIENT. MANUFACTURER RESPONSE FOR X-RAY LAP SPONGE, BILATERAL KNEE PACK (PER SITE REPORTER) ACCORDING TO REPORT, MANUFACTURER NOTIFIED.

Description of Event or Problem · 0

BILATERAL KNEE PACK CONTENTS LISTED AS CONTAINING 4 PACKS OF X-RAY LAP SPONGES. WHEN PACK OPENED, ONLY 3 PACKS OF X-RAY LAP SPONGES PRESENT. ISSUE FOUND AND RESOLVED PRIOR TO PATIENT ENTERING OR. CHARGE RN AND MATERIALS AWARE. NO HARM TO PATIENT. MANUFACTURER RESPONSE FOR X-RAY LAP SPONGE, BILATERAL KNEE PACK (PER SITE REPORTER) ACCORDING TO REPORT, MANUFACTURER NOTIFIED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
913578 BILATERAL KNEE PACK ORTHOPEDIC TRAY OJH CARDINAL HEALTH 200, LLC PO4EBKSRK 855067

Patients

Seq Age Sex Outcome Treatment
1 Unknown