# FDA recall Z-1870-2021

> **Siemens Healthcare Diagnostics, Inc.** · Class II · device recall initiated 2021-05-04.

## Product

Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676)  Siemens Material Number: 11067000

## Reason for recall

Photometer Lamp May Reach Saturation Without Flagging Results, may  generate erroneously elevated or depressed patient results

## Distribution

Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Bulgaria, Burkina Faso, Canada, Chile, Colombia, Croatia  Cura¿ao, Czech Republic, Denmark, Ecuador, Egypt, Estonia, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Kenya, Kuwait, Latvia, Libya, Lithuania, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Nigeria, Norway, Oman, P.R. China  Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Republic Korea, Romania, Russian Fed., Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, U.A.E., Uganda, United Kingdom, Uruguay, Vatikancity, Vietnam.

## Key facts

- **Recall number:** Z-1870-2021
- **Recalling firm:** Siemens Healthcare Diagnostics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-05-04
- **Report date:** 2021-06-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tarrytown, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1870-2021

## Citation

> AI Analytics. FDA recall Z-1870-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1870-2021. Source: US FDA. Licensed CC0.

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