FDA Adverse Event Malfunction Summary report: N

18 CM (7") PRESSURE INFUSION (400PSIG) EXT SET W/MICROCLAVE® CLEAR, ROTATING LUE

MDR report key: 14780597 · Received June 22, 2022

Report

Report Number
9617594-2022-00186
Event Type
Malfunction
Date Received
June 22, 2022
Date of Event
May 4, 2022
Report Date
June 13, 2022
Manufacturer
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.
Product Code
FPA
UDI-DI
00840619081591
PMA / PMN Number
K100576
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE WAS RETURNED TO ICU MEDICAL, INC FOR EVALUATION. ICU MEDICAL, INC ENGINEERING SIGNED OFF ON THE COMPLETED EVALUATION. THE DEVICE WAS OPENED BUT UNUSED.

Description of Event or Problem · 0

THE CUSTOMER REPORTED A SEPARATED PRESSURE TUBING TO ICU MEDICAL INC AND AN INITIAL EMDR WAS SUBMITTED BY THE MANUFACTURER UNDER MFR REPORT REF #9617594-2022-00081-00. THE CUSTOMER RETURNED THE ORIGINAL DEVICE FOR EVALUATION, BUT ALSO RETURNED AN ADDITIONAL OPEN/UNUSED DEVICE 18 CM (7") PRESSURE INFUSION (400PSIG) EXT SET W/MICROCLAVE® CLEAR, ROTATING LUER FOR EVALUATION ON (B)(6) 2022. A PULL TEST WAS PERFORMED ON THE REPRESENTATIVE TUBING/MALE LUER ADAPTOR BOND OF THE UNUSED SAMPLE AND IT FAILED. SOME SOLVENT WAS PRESENT ON THE TUBING. NO OTHER DAMAGE OR ANOMALIES WERE IDENTIFIED. THE SAMPLE FAILED TO MEET THE BOND INTEGRITY REQUIREMENTS. THE PROBABLE CAUSE IS DUE TO A BONDING ERROR DURING MANUFACTURING. THE LOT HISTORY WAS REVIEWED AND NO NONCONFORMITIES WERE IDENTIFIED THAT MAY HAVE CONTRIBUTED TO THE REPORTED COMPLAINT. THIS IS REPORT 2 OF 3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1456149 18 CM (7") PRESSURE INFUSION (400PSIG) EXT SET W/MICROCLAVE® CLEAR, ROTATING LUE SET, ADMINISTRATION, INTRAVASCULAR FPA ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V. 5800251 00840619081591

Patients

Seq Age Sex Outcome Treatment
1 Unknown