# FDA recall Z-2400-2026

> **Inter-Med Llc** · Class II · device recall initiated 2026-05-27.

## Product

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28

## Reason for recall

Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.

## Distribution

US Nationwide distribution in the states of Tennessee and Missouri.

## Key facts

- **Recall number:** Z-2400-2026
- **Recalling firm:** Inter-Med Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-27
- **Report date:** 2026-06-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Racine, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2400-2026

## Citation

> MORVS. FDA recall Z-2400-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2400-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*