# FDA recall Z-0922-2022

> **Abbott Vascular** · Class II · device recall initiated 2022-03-11.

## Product

20/30 Priority Pack Accessory Kit/.096 RHV  - REF 1000186 WPL2122270-01 (2019-03-01)    20/30 Priority Pack w/.115 RHV - REF 1000186-115 WPL2122270-02 (2019-03-01)

## Reason for recall

Due to an increase in complaint trend for leaks and intermittent/loose connections.

## Distribution

U.S Nationwide Distribution.: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, SC, TN, TX, VA, WA, and WI.    O.U.S.: United Arab Emirates, France, Pakistan, Argentina, United Kingdom, Portugal, Australia, Greece, R¿union, Belgium, Guam, Romania, Brazil, Indonesia, Russian Federation,  Bahamas, Israel, Saudi Arabia, Canada, India, Singapore, Switzerland, Italy, Slovakia, Chile, Jamaica, Thailand, China, Japan, Taiwan Republic of China, Colombia, Korea (South), Costa Rica, Luxembourg, Uruguay, Czech Republic, Mexico, Vietnam, Germany, Netherlands, South Africa, Dominican Republic, New Zealand, Spain, and Panama

## Key facts

- **Recall number:** Z-0922-2022
- **Recalling firm:** Abbott Vascular
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-03-11
- **Report date:** 2022-04-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0922-2022

## Citation

> AI Analytics. FDA recall Z-0922-2022. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-0922-2022. Source: US FDA. Licensed CC0.

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