Cardiovascular Procedure Kit 76623Recalls & reported problems

Terumo Cardiovascular Systems Corporation

All models of Cardiovascular Procedure Kit (227)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00699753511064), received between Apr 25, 2020 and Apr 25, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Disconnection” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

Disconnection1

Patient problems

Blood Loss1
No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryApr 25, 2020Disconnection; Disconnection
THE CUSTOMER REPORTED THAT DURING CARDIOPULMONARY BYPASS (CPB) PROCEDURE, THE CONNECTION BETWEEN THE 1/2" ARTERIAL ROLLER PUMP BOOT AND CONNECTOR, DISCONNECTED. THE DISCONNECTION RESULTED IN APPROXIMATELY 500 MILLILITERS (ML) BLOOD LOSS. THE PRODUCT WAS CHANGED OUT AFTER THE BYPASS WAS TERMINATED. THE SURGERY WAS COMPLETED, WITH THE ONLY CHANGE TO THE PRACTICE WAS THAT THE BYPASS WAS TERMINATED 10-15 MINUTES EARLIER THAN PLANNED.
Patient problems: Blood Loss; No Consequences Or Impact To Patient
MAUDE report 9999263 ↗

Device details

UDI-DI	`00699753511064`
Brand	Cardiovascular Procedure Kit
Model	76623
Company	Terumo Cardiovascular Systems Corporation
Product code	—
Class	—
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 8, 2022

Device type (GMDN): Cardiopulmonary bypass system blood tubing set

A collection of sterile devices including tubing and typically clamps, filters, connectors, and stopcocks, used in a circuit for a cardiopulmonary bypass procedure. The tubing is typically polymeric and may be heparin coated. It is typically used in the blood pump head of a cardiopulmonary bypass system. The tubing, when used in a roller type pump, will be cyclically compressed by the blood pump to cause the blood to flow through the heart-lung bypass system. This is a single-use device.

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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