# FDA recall Z-0294-2021

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-09-14.

## Product

Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media  Ref: P6153118

## Reason for recall

Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.

## Distribution

Foreign:  Italy, Spain, and UK

## Key facts

- **Recall number:** Z-0294-2021
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-14
- **Report date:** 2020-11-04
- **Termination date:** 2021-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0294-2021

## Citation

> AI Analytics. FDA recall Z-0294-2021. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0294-2021. Source: US FDA. Licensed CC0.

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