# FDA recall Z-0002-2022

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2021-07-27.

## Product

REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

## Reason for recall

Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of  AL, AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NE, NH, NJ, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WV and the countries of Netherlands, United Arab Emirates, Australia, Taiwan, Asia, South Africa, Canada, JAPAN, India, Hong Kong, New Zealand,  Mexico, China, Belgium, Malaysia, Singapore, Vietnam.

## Key facts

- **Recall number:** Z-0002-2022
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-07-27
- **Report date:** 2021-10-13

- **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-0002-2022

## Citation

> AI Analytics. FDA recall Z-0002-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0002-2022. Source: US FDA. Licensed CC0.

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