# FDA recall Z-1994-2021

> **Bard Access Systems Inc.** · Class II · device recall initiated 2021-05-19.

## Product

5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire    Unit Label:  PowerPICC REF CK000340B  BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire

## Reason for recall

Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.

## Distribution

U.S. Nationwide distribution in the state of RI.

## Key facts

- **Recall number:** Z-1994-2021
- **Recalling firm:** Bard Access Systems Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-05-19
- **Report date:** 2021-07-07
- **Termination date:** 2023-03-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1994-2021

## Citation

> AI Analytics. FDA recall Z-1994-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1994-2021. Source: US FDA. Licensed CC0.

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