# FDA recall Z-1384-2022

> **Agilent Technologies, Inc.** · Class III · device recall initiated 2022-05-20.

## Product

Kit Label:  Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2  Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21    Vial Labels:  Mat. No K589911-21512

## Reason for recall

Label provided for substrate vail contained incorrect expiration date.

## Distribution

U.S. Nationwide distribution in the states of NY and VA.

## Key facts

- **Recall number:** Z-1384-2022
- **Recalling firm:** Agilent Technologies, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-20
- **Report date:** 2022-07-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1384-2022

## Citation

> AI Analytics. FDA recall Z-1384-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1384-2022. Source: US FDA. Licensed CC0.

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