# FDA recall Z-0714-2024

> **Ambu Inc.** · Class II · device recall initiated 2023-12-05.

## Product

Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2

## Reason for recall

Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14   16 mm when mounting Ambu aView 2 Advance on a VESA interface. Using longer screw lengths will penetrate the lithium-ion battery and result in a fire hazard and battery leakage which can cause severe burns, smoke inhalation and skin irritation. Using shorter screw lengths could result in unsecure device fastening.

## Distribution

Domestic distribution nationwide.

## Key facts

- **Recall number:** Z-0714-2024
- **Recalling firm:** Ambu Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-05
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbia, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0714-2024

## Citation

> AI Analytics. FDA recall Z-0714-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0714-2024. Source: US FDA. Licensed CC0.

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