# FDA recall Z-1946-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-03-17.

## Product

PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length  Catalog Number: ST018101D

## Reason for recall

Iincorrectly packaged without the required lidocaine as labeled

## Distribution

AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),

## Key facts

- **Recall number:** Z-1946-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-17
- **Report date:** 2020-05-20
- **Termination date:** 2020-10-21

- **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-1946-2020

## Citation

> AI Analytics. FDA recall Z-1946-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1946-2020. Source: US FDA. Licensed CC0.

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