# FDA recall Z-2526-2026

> **PFM MEDICAL INC.** · Class II · device recall initiated 2026-04-21.

## Product

Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310

## Reason for recall

A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.

## Distribution

US Nationwide distribution in the states of NY, MD.

## Key facts

- **Recall number:** Z-2526-2026
- **Recalling firm:** PFM MEDICAL INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-21
- **Report date:** 2026-07-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2526-2026

## Citation

> MORVS. FDA recall Z-2526-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2526-2026. Source: US FDA. Licensed CC0.

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