# FDA recall Z-0791-2022

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2022-01-20.

## Product

LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5

## Reason for recall

Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

## Distribution

U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, 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. (foreign) including states: Costa Rica and Hong Kong.

## Key facts

- **Recall number:** Z-0791-2022
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-20
- **Report date:** 2022-03-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0791-2022

## Citation

> AI Analytics. FDA recall Z-0791-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0791-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*