# FDA recall Z-1251-2025

> **HUMAN MED AG** · Class II · device recall initiated 2024-10-18.

## Product

human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.

## Reason for recall

The cannula tubes do not comply with the specification.  The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spray jet.

## Distribution

US Nationwide distribution in the state of  FL.

## Key facts

- **Recall number:** Z-1251-2025
- **Recalling firm:** HUMAN MED AG
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-18
- **Report date:** 2025-03-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Schwerin, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1251-2025

## Citation

> AI Analytics. FDA recall Z-1251-2025. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-1251-2025. Source: US FDA. Licensed CC0.

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