FDA Adverse Event Malfunction Summary report: N

CARDINAL HEALTH

MDR report key: 19095081 · Received April 12, 2024

Report

Report Number
3005670221-2024-00011
Event Type
Malfunction
Date Received
April 12, 2024
Report Date
April 12, 2024
Manufacturer
JIANGSU CAINA MEDICAL CO., LTD.
Product Code
FMF
PMA / PMN Number
K113091
Removal / Correction Number
Z-0855-2024
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

RETURNED SAMPLE WAS REQUESTED BUT HAVEN'T RECEIVED YET. THE DHR OF THIS LOT WAS REVIEWED WITHOUT ANY ISSUE. THE DESIGN HISTORY FILE AND 510K SUBMISSION WERE REVIEWED. THIS SYRINGE IS DESIGNED FOR MANUAL USE ONLY, NOT FOR PUMP USE. FOR MANUAL USE OR NOT FOR PUMP USE WAS NOT PRESENTED ON ANY LABELING OF THIS PRODUCT. THE COMPLIANT HISTORY WAS REVIEW NO PUMP COMPATABILITY ISSUES WITH THIS PRODUCT WERE RECEIVED BEFORE. A RECALL WAS CONDUCTED BY DISTRIBUTOR CARDINAL HEALTH 200 LLC WITH RECALL NUMBER Z-0855-2024. THE CORRECTIVE ACTION PUTTING THE CAUTION "FOR MANUAL USE OR NOT FOR PUMP USE" ON ALL SYRINGES' LABELING OF (B)(6) WILL BE TAKEN. A FOLLOW-UP REPORT WILL BE SUBMITTED IF ANY ADDITIONAL INFORMATION FROM THE RECEIVED SAMPLES.

Description of Event or Problem · 0

CUSTOMER REPORTS: WE HAVE DISCOVERED THAT WHEN CARDINAL CHANGED THE SYRINGE FROM COVIDIEN BRAND TO THE CARDINAL BRAND THEY CHANGED THE SPECIFICATIONS OF THE SYRINGE. THIS SYRINGE IS CALIBRATED TO A SMITH MEDICAL SYRINGE PUMP USED IN THE OR,ICU AND NICU. THE PUMP WILL NOT RECOGNIZE THE SYRINGE BECAUSE IT IS 1-2 MM NARROWER THAN THE COVIDIEN SYRINGE. IS THERE ANY SOLUTION TO THIS PROBLEM?

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
779625 CARDINAL HEALTH SYRINGE FMF JIANGSU CAINA MEDICAL CO., LTD.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other