No image published for this recall

Maquet Cardiopulmonary - safety alert

Official notice

4 Jun 2025

MediumFDA

An official FDA notice concerns Maquet Cardiopulmonary. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-06-04. Recall numbers: Z-1823-2025. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

2

Recall number

Z-1823-2025

Official notice

2025-06-04

The hazard

Health risk requiring medical assessment

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

96820

Recall Numbers

Z-1823-2025

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · IL

Location 2

US · United States · MO

Affected area 1

US · United States

Affected area 2

AT · Austria

Affected area 3

AU · Australia

Affected area 4

BE · Belgium

Affected area 5

CA · Canada

Affected area 6

CH · Switzerland

Affected area 7

CN · China

Affected area 8

CO · Colombia

Affected area 9

CZ · Czech Republic

Affected area 10

DE · Germany

Affected area 11

DK · Denmark

Affected area 12

ES · Spain

Affected area 13

FI · Finland

Affected area 14

FR · France

Affected area 15

HR · Croatia

Affected area 16

IL · Israel

Affected area 17

IN · India

Affected area 18

IT · Italy

Affected area 19

JP · Japan

Affected area 20

KR · South Korea

Affected area 21

PL · Poland

Affected area 22

RU · Russia

Affected area 23

SA · Saudi Arabia

Affected area 24

TH · Thailand

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Maquet Cardiopulmonary. Contact: Maquet Cardiopulmonary Ag.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-1823-2025

Event id

96820

Units affected

2

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

ELECTRONICS
Medium

Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS) - safety alert

FDA23 Sept 2026

Brand match

Medium risk

Markets

AU
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA6 Aug 2025

Brand match

Medium risk

Markets

AU
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA16 May 2018

Brand match

Medium risk

Markets

US

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 4 Jun 2025. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.