# FDA recall Z-3129-2024

> **Medical Action Industries, Inc. 306** · Class II · device recall initiated 2024-06-11.

## Product

Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 each/case), 6141 (250 each/case), 6203 (40 each/case), 6805 (50 each/case), 6805-1 (175 each/case), 6810 (50 each/case), 6810-1 (350 each/case), 6830 (8 rolls/case), and 6860 (8 rolls/case)

## Reason for recall

The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code.  These blue foam pouches were misused due to misclassification of the GMDN.

## Distribution

Nationwide distribution.  International distribution to Canada.

## Key facts

- **Recall number:** Z-3129-2024
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-11
- **Report date:** 2024-09-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arden, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3129-2024

## Citation

> AI Analytics. FDA recall Z-3129-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-3129-2024. Source: US FDA. Licensed CC0.

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