# FDA recall Z-2065-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-04-16.

## Product

BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535

## Reason for recall

This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.

## Distribution

Nationwide domestic distribution. Foreign distribution to Austria, Belgium, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, UK, Australia, Canada, Mexico, Malaysia, New Zealand

## Key facts

- **Recall number:** Z-2065-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-16
- **Report date:** 2020-05-27
- **Termination date:** 2021-09-01

- **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-2065-2020

## Citation

> AI Analytics. FDA recall Z-2065-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2065-2020. Source: US FDA. Licensed CC0.

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