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Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223

Official notice

7 Oct 2026

Last checked

13 Oct 2026

MediumFDA

An official FDA notice concerns Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2026-10-07. Recall numbers: Z-3335-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

42,940

Recall number

Z-3335-2026

Official notice

2026-10-07

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.

Other

UDI-DI 00630414610887

Event Ids

99726

Recall Numbers

Z-3335-2026

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Affected products

Product 1

Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223

Units affected

42,940

Risk / hazard

Health risk requiring medical assessment

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

AR · Argentina

Affected area 3

AT · Austria

Affected area 4

AU · Australia

Affected area 5

BE · Belgium

Affected area 6

BG · Bulgaria

Affected area 7

BR · Brazil

Affected area 8

CA · Canada

Affected area 9

CH · Switzerland

Affected area 10

CL · Chile

Affected area 11

CN · China

Affected area 12

CZ · Czech Republic

Affected area 13

DE · Germany

Affected area 14

DK · Denmark

Affected area 15

EE · Estonia

Affected area 16

EG · Egypt

Affected area 17

ES · Spain

Affected area 18

FI · Finland

Affected area 19

FR · France

Affected area 20

GB · United Kingdom

Affected area 21

GR · Greece

Affected area 22

HK · Hong Kong

Affected area 23

HR · Croatia

Affected area 24

HU · Hungary

Affected area 25

IE · Ireland

Affected area 26

IL · Israel

Affected area 27

IN · India

Affected area 28

IT · Italy

Affected area 29

JO · Jordan

Affected area 30

KR · South Korea

Affected area 31

KW · Kuwait

Affected area 32

LT · Lithuania

Affected area 33

LV · Latvia

Affected area 34

MX · Mexico

Affected area 35

MY · Malaysia

Affected area 36

NL · Netherlands

Affected area 37

NO · Norway

Affected area 38

NZ · New Zealand

Affected area 39

PE · Peru

Affected area 40

PK · Pakistan

Affected area 41

PL · Poland

Affected area 42

PT · Portugal

Affected area 43

RO · Romania

Affected area 44

RS · Serbia

Affected area 45

SA · Saudi Arabia

Affected area 46

SE · Sweden

Affected area 47

SG · Singapore

Affected area 48

SI · Slovenia

Affected area 49

SK · Slovakia

Affected area 50

SV · El Salvador

Affected area 51

TH · Thailand

Affected area 52

TR · Turkey

Affected area 53

TW · Taiwan

Affected area 54

UY · Uruguay

Affected area 55

VN · Vietnam

Affected area 56

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-3335-2026

Event id

99726

Units affected

42,940

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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