# FDA recall Z-0284-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-04-10.

## Product

MaxZero Extension Sets with Needle-less Connector, Product codes MZ1000  MZ1000-07			MZ5301  MZ5302			MZ5303  MZ5304			MZ5305  MZ5306			MZ5307  MZ5309			MZ5310  MZ5312			MZ5313  MZ5316			MZ8001  MZ8002			MZ8003  MZ9266			MZ9267  			  MZ9272			MZ9273  MZ9274			MZ9275  MZ9276			MZ9277  MZ9278			MZ9279  MZ9280			MZ9281  MZ9283			MZ9287  MZ9288			MZ9289  MZ9290			MZ9292  MZ9293			MZ9294  MZ9300			MZ9301  MZ9302			MZ9313  			  MZ9323			MZ9324  MZ9325			MZ9326  MZ9327			MZ9329  MZT1003			MZT1004  MZX5302			MZXT5303  MZXT5304			MZX5305  MZX5306			MZXT5306  MZXT5307			MZXT9001  MZXT9003			MZXT9004

## Reason for recall

BD has decided to initiate a voluntary recall due to a confirmed complaint trend for  droplets of fluid separating from the sealed surface of the MaxZero connector, following  disconnection.

## Distribution

Nationwide domestic distribution. Foreign distribution to Argentina  Australia  Austria  Belgium  Brazil  Canada  Chile  China  Colombia  Croatia  Cyprus  Czech Republic  Denmark  Finland  France  Germany  Hungary  India  Italy  Japan  Jordan  Kuwait  Lebanon  Mexico  Morocco  Netherlands  Norway  Oman  Poland  Qatar  Saudi Arabia  Singapore  Slovenia  South Korea  Spain  Sweden  Switzerland  Thailand  Turkey  UAE  United Kingdom.

## Key facts

- **Recall number:** Z-0284-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-10
- **Report date:** 2019-11-13
- **Termination date:** 2020-12-22

- **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-0284-2020

## Citation

> AI Analytics. FDA recall Z-0284-2020. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-0284-2020. Source: US FDA. Licensed CC0.

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