# FDA recall Z-2407-2024

> **Ethicon Sarl, a Johnson & Johnson Company** · Class II · device recall initiated 2024-06-11.

## Product

SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963

## Reason for recall

Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.

## Distribution

Worldwide distribution - US Nationwide and the countries of India and Japan.

## Key facts

- **Recall number:** Z-2407-2024
- **Recalling firm:** Ethicon Sarl, a Johnson & Johnson Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-11
- **Report date:** 2024-07-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Neuchatel, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2407-2024

## Citation

> AI Analytics. FDA recall Z-2407-2024. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-2407-2024. Source: US FDA. Licensed CC0.

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