# FDA recall Z-1555-2022

> **Becton Dickinson & Company** · Class II · device recall initiated 2022-07-18.

## Product

BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system.  Catalog Number:  515304

## Reason for recall

Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.

## Distribution

US Nationwide Distribution  CA  FL  GA  IL  MD  MI  OR  PA  PR  TN  TX

## Key facts

- **Recall number:** Z-1555-2022
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-18
- **Report date:** 2022-08-24

- **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-1555-2022

## Citation

> AI Analytics. FDA recall Z-1555-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1555-2022. Source: US FDA. Licensed CC0.

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