FDA Device recall Z-2272-2018
Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020
- FDA Device
- Class II
- terminated
- Published 2018-06-27
On 2018-06-27 the FDA classified a Class II recall of Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020 by Cryolife, citing devices, which met FDA and AATB eligibility criteria, were distributed. Final autopsy and toxicology reports indicated the presence of morphine in the urine.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2272-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-14 |
| Published | 2018-06-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cryolife |
| Distribution | AR, OH |
Product
Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020
Reason
Devices, which met FDA and AATB eligibility criteria, were distributed. Final autopsy and toxicology reports indicated the presence of morphine in the urine.
Identifiers
| code_info | Serial Number 10988328 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2272-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.