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Recall Observatory FDA recall evidence

Device product

Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020

Z-2272-2018

May 14, 2018

Class II

Product summary

Firm
CryoLife, Inc.
Event
Event 80199
Status
Terminated
Classification
Class II
Quantity
1 unit
Official record key
device-enforcement:Z-2272-2018

Official wording

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

Code information: Serial Number 10988328

Distribution pattern: AR, OH

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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