# FDA recall Z-0365-2020

> **Cadence Science, Inc.** · Class II · device recall initiated 2019-05-10.

## Product

Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404);  5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use

## Reason for recall

The glass syringe used with Pressure Control Syringes may potentially break during use.

## Distribution

US Nationwide distribution in the states of AL, AR, CA, FL, GA, IA, ID, IL, MO, NH, NJ, NY, OH, PA, SC, TX, VA, and WI.

## Key facts

- **Recall number:** Z-0365-2020
- **Recalling firm:** Cadence Science, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-10
- **Report date:** 2019-11-20
- **Termination date:** 2020-06-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cranston, RI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0365-2020

## Citation

> AI Analytics. FDA recall Z-0365-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0365-2020. Source: US FDA. Licensed CC0.

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