# FDA recall Z-1722-2022

> **ICU Medical, Inc.** · Class II · device recall initiated 2022-08-01.

## Product

MicroClave Clear Neutral Connector;    MicroClave Clear Connector;    MicroClave Clear Neutral Connector, Approx Priming Volume: 0.04 mL.   Accessory for Intravascular Administration Set

## Reason for recall

Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.

## Distribution

U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, 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, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY.  O.U.S.: Austria, Bahrain, Belgium, Canada, Colombia, Estonia, France, Germany, Ireland, Israel, Italy, Japan, Kuwait, Luxembourg, Malaysia, Peru, Poland, Saudi Arabia, Slovakia, Slovenia, Spain, Sweden, Thailand, Turkey, United Arab Emirates, United Kingdom, and Vietnam.  O.U.S.

## Key facts

- **Recall number:** Z-1722-2022
- **Recalling firm:** ICU Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-01
- **Report date:** 2022-09-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Clemente, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1722-2022

## Citation

> AI Analytics. FDA recall Z-1722-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1722-2022. Source: US FDA. Licensed CC0.

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