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Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic

Official notice

12 Aug 2026

Last checked

22 Sept 2026

MediumFDA

An official FDA notice concerns Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic. The notice reports a chemical exposure risk. Stop using the product and follow the official notice. Published 2026-08-12. Recall numbers: Z-2890-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

7,018

Recall number

Z-2890-2026

Official notice

2026-08-12

The hazard

Chemical exposure risk

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

99389

Recall Numbers

Z-2890-2026

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Affected products

Product 1

Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic

Units affected

7,018

Risk / hazard

Chemical exposure risk

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

Affected area 1

US · United States

Affected area 2

AT · Austria

Affected area 3

AU · Australia

Affected area 4

BE · Belgium

Affected area 5

BR · Brazil

Affected area 6

CA · Canada

Affected area 7

CH · Switzerland

Affected area 8

CL · Chile

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

GR · Greece

Affected area 16

HK · Hong Kong

Affected area 17

IE · Ireland

Affected area 18

IL · Israel

Affected area 19

IT · Italy

Affected area 20

KR · South Korea

Affected area 21

LV · Latvia

Affected area 22

MY · Malaysia

Affected area 23

NL · Netherlands

Affected area 24

NO · Norway

Affected area 25

NZ · New Zealand

Affected area 26

PT · Portugal

Affected area 27

RO · Romania

Affected area 28

SE · Sweden

Affected area 29

SG · Singapore

Affected area 30

SI · Slovenia

Affected area 31

SK · Slovakia

Affected area 32

ZA · South Africa

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Siemens Healthcare Diagnostics. Contact: Siemens Healthcare Diagnostics, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-2890-2026

Event id

99389

Units affected

7,018

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
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