# FDA recall Z-1923-2026

> **Remel Europe Ltd.** · Class II · device recall initiated 2026-03-25.

## Product

Oxoid Agglutinating Sera, Salmonella 9-0  R30957301

## Reason for recall

Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.

## Distribution

Worldwide - US Nationwide distribution to the states of AL, CA, FL, IA, IL, IN, MI, MN, MO, NC, NE, OH, SD, TX, WA.

## Key facts

- **Recall number:** Z-1923-2026
- **Recalling firm:** Remel Europe Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-25
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dartford, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1923-2026

## Citation

> AI Analytics. FDA recall Z-1923-2026. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-1923-2026. Source: US FDA. Licensed CC0.

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