# FDA recall Z-2272-2018

> **CryoLife, Inc.** · Class II · device recall initiated 2018-05-14.

## Product

Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020

## Reason for recall

Devices, which met FDA and AATB eligibility criteria, were distributed.  Final autopsy and toxicology reports indicated the presence of morphine in the urine.

## Distribution

AR, OH

## Key facts

- **Recall number:** Z-2272-2018
- **Recalling firm:** CryoLife, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-14
- **Report date:** 2018-06-27
- **Termination date:** 2019-03-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kennesaw, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2272-2018

## Citation

> AI Analytics. FDA recall Z-2272-2018. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2272-2018. Source: US FDA. Licensed CC0.

---

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