# FDA recall Z-2176-2025

> **B BRAUN MEDICAL INC** · Class I · device recall initiated 2025-07-09.

## Product

Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.

## Reason for recall

Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent, which is common to air eliminating filters.

## Distribution

US distribution to AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, WA, WY.  International distribution to Canada.

## Key facts

- **Recall number:** Z-2176-2025
- **Recalling firm:** B BRAUN MEDICAL INC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-09
- **Report date:** 2025-08-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allentown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2176-2025

## Citation

> AI Analytics. FDA recall Z-2176-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2176-2025. Source: US FDA. Licensed CC0.

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