# FDA recall Z-1474-2026

> **Remel, Inc** · Class II · device recall initiated 2026-02-05.

## Product

Campy CVA Medium 100/PK, R01272

## Reason for recall

Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

## Distribution

US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.

## Key facts

- **Recall number:** Z-1474-2026
- **Recalling firm:** Remel, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-05
- **Report date:** 2026-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lenexa, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1474-2026

## Citation

> AI Analytics. FDA recall Z-1474-2026. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-1474-2026. Source: US FDA. Licensed CC0.

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