# FDA recall Z-0285-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-09-16.

## Product

13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023    Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.

## Reason for recall

A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.

## Distribution

Distributed to healthcare facilities in AR, FL, IL, NJ, TX, and WI.

## Key facts

- **Recall number:** Z-0285-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-09-16
- **Report date:** 2019-11-13
- **Termination date:** 2020-06-29

- **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-0285-2020

## Citation

> AI Analytics. FDA recall Z-0285-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0285-2020. Source: US FDA. Licensed CC0.

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