# FDA recall Z-0100-2020

> **Centurion Medical Products Corporation** · Class II · device recall initiated 2019-04-24.

## Product

OR VANTEX 7FR 3L 16CM CVC  ECVC6665

## Reason for recall

Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.

## Distribution

Nationwide domestic distribution.

## Key facts

- **Recall number:** Z-0100-2020
- **Recalling firm:** Centurion Medical Products Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-24
- **Report date:** 2019-10-16
- **Termination date:** 2020-04-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Williamston, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0100-2020

## Citation

> AI Analytics. FDA recall Z-0100-2020. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-0100-2020. Source: US FDA. Licensed CC0.

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