# FDA recall Z-1169-2018

> **Beckman Coulter Inc.** · Class II · device recall initiated 2018-01-19.

## Product

AutoMate 1200 Catalog Number ODL25120;  AutoMate 1250 Catalog Number ODL25125;  AutoMate 2500 Catalog Number ODL25250;  AutoMate 2550 Catalog Number ODL25255

## Reason for recall

Belts on the x-axis (and on the y-axis, to a lesser extent) manufactured from 2015 are showing premature failure, posing the remote risk of cross-contamination.

## Distribution

Australia, Austria, Belarus,  Belgium, Bosnia and Herzegovina, Brazil,  Canada, China, Croatia,  Cyprus, Czech Republic, Denmark,  Finland, France, Germany,  Gibraltar, Greece, Hong Kong,  Hungary, India, Ireland,  Israel, Italy, Korea,  Kuwait, Latvia, Lithuania,  Macao, Mayotte, Mexico,  Netherlands, New Zealand, Norway,  Panama, Poland, Portugal,  Qatar, Russia, Saudi Arabia,  Singapore, Slovakia, Slovenia,  South Africa, Spain, Sweden,  Switzerland, Taiwan, Turkey,  United Kingdom, United States

## Key facts

- **Recall number:** Z-1169-2018
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2018-01-19
- **Report date:** 2018-03-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brea, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1169-2018

## Citation

> AI Analytics. FDA recall Z-1169-2018. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1169-2018. Source: US FDA. Licensed CC0.

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