# FDA recall Z-1723-2019

> **Cook Inc.** · Class II · device recall initiated 2019-04-09.

## Product

Pericardiocentesis Catheter Tray, RPN C-PCYS-850, Order # G03284

## Reason for recall

Affected products may have been manufactured with the catheter distal end hole too small

## Distribution

Domestically: OH;     Internationally: CANADA, SPAIN, ITALY, BELGIUM, GERMANY, UNITED ARAB EMIRATES, GREECE, SWITZERLAND, OMAN, MONACO, SAUDI ARABIA,  AUSTRALIA, HONG KONG, INDIA & KOREA

## Key facts

- **Recall number:** Z-1723-2019
- **Recalling firm:** Cook Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-09
- **Report date:** 2019-06-12
- **Termination date:** 2020-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bloomington, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1723-2019

## Citation

> AI Analytics. FDA recall Z-1723-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1723-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*