# FDA recall Z-2247-2021

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2021-06-23.

## Product

TJM6008	Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm;  TJC3513	Jamshidi" Bone Marrow Biopsy/Aspiration Needle. 13G x 8.9 cm;  TJM4011	Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 11G x 10cm;  TJC4011	Jamshidi" Bone Marrow Biopsy/Aspiration Needle. 11G x 10cm;  TJM4008	Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 10cm;  TJC4008	Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 10cm;

## Reason for recall

Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.

## Distribution

U.S Nationwide Distribution in the states of .: AZ, CT, DC, FL, IL, MA, MI, MO, NY, OK, TX, and VA    O.U.S.: Australia, Belgium, China, EMEA, Japan, Mexico, Saudi Arabia, Singapore, Taiwan

## Key facts

- **Recall number:** Z-2247-2021
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-06-23
- **Report date:** 2021-08-18

- **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-2247-2021

## Citation

> AI Analytics. FDA recall Z-2247-2021. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-2247-2021. Source: US FDA. Licensed CC0.

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