FDA Adverse Event Malfunction Summary report: N

RED 4-CHANNEL HPT CARTRIDGE WITH PORCINE

MDR report key: 24144096 · Received January 22, 2026

Report

Report Number
2184009-2026-00143
Event Type
Malfunction
Date Received
January 22, 2026
Date of Event
June 28, 2023
Report Date
January 22, 2026
Manufacturer
MEDTRONIC BLOOD MANAGEMENT
Product Code
JOX
PMA / PMN Number
K894317
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS REGULATORY REPORT IS BEING SUBMITTED AS PART OF A RETROSPECTIVE REVIEW AND REMEDIATION AS PART OF A CAPA ACTION. MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF HR-ACT CARTRIDGES AND HMS RED CARTRIDGES, THE CUSTOMER REPORTED THAT THE PRODUCT WAS DELIVERED IN A DAMAGED, WET BOX. THE DEVICE WAS REPLACED. THERE WAS NO ADVERSE PATIENT EFFECT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THERE WEREN'T ANY MISSING OR WRONG DEVICES OR COMPONENTS IN THE PACKAGE. THE OUTER BOX WAS DAMAGED, THE STERILE SEAL WAS DAMAGED AND PRODUCT WAS LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
203922 RED 4-CHANNEL HPT CARTRIDGE WITH PORCINE ANALYZER, HEPARIN, AUTOMATED JOX MEDTRONIC BLOOD MANAGEMENT 304-01POR UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown