# FDA recall Z-0072-2025

> **Merit Medical Systems, Inc.** · Class II · device recall initiated 2024-08-19.

## Product

basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C

## Reason for recall

Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.

## Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and the countries of  France, Italy, Jamaica, Ireland, Paraguay, Australia, India, Nepal, Japan.

## Key facts

- **Recall number:** Z-0072-2025
- **Recalling firm:** Merit Medical Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-19
- **Report date:** 2024-10-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** South Jordan, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0072-2025

## Citation

> AI Analytics. FDA recall Z-0072-2025. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0072-2025. Source: US FDA. Licensed CC0.

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