FDA recall Z-1956-2020

Merit Medical Systems, Inc. · Class II · device

Product

Custom Sheath Introducer Kit REF K21-00031 - Product Usage: intended use is to provide access and facilitate the percutaneous introduction of various devices into vein.

Reason for recall

labeling error: Due to a manufacturing issue, product package was incorrectly labeled with the incorrect sheath size and the incorrect sheath assembly was included in the product packaging. The use of the incorrect kit components may result in vasoconstriction, moderate hemorrhage, and/or embolism.

Distribution

US Nationwide distribution in the state of MI.

Key facts

Status
Terminated
Initiation date
2019-09-12
Report date
2020-05-20
Termination date
2022-05-27
Voluntary/Mandated
Voluntary: Firm initiated
Location
South Jordan, UT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1956-2020