# FDA recall Z-3106-2026

> **Medical Action Industries, Inc. 306** · Class I · device recall initiated 2026-07-23.

## Product

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

## Reason for recall

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

## Distribution

US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

## Key facts

- **Recall number:** Z-3106-2026
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-23
- **Report date:** 2026-09-16

- **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-3106-2026

## Citation

> MORVS. FDA recall Z-3106-2026. Retrieved 2026-10-22 from https://api.morvs.ai/recall/Z-3106-2026. Source: US FDA. Licensed CC0.

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