# FDA recall Z-1875-2026

> **Angiodynamics, Inc.** · Class II · device recall initiated 2026-03-03.

## Product

AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers;  ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM;  Catalog No.: 13709804;  Product/UPN No.: H787137098045 (Box), H787137098040 (Pouch);  Box Quantity: 5 pouches;

## Reason for recall

The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.

## Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon, Netherlands, New Zealand, Panama, Slovenia, South Africa, Spain, Sweden, Thailand.

## Key facts

- **Recall number:** Z-1875-2026
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-03
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Queensbury, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1875-2026

## Citation

> AI Analytics. FDA recall Z-1875-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1875-2026. Source: US FDA. Licensed CC0.

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