FDA-Device2023-06-21Class II
Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Galt Medical Corporation
Hazard
Sheath introducer assemblies could potentially, due to improper storage conditions, have a luer connection portion of the dilator hub that cracks or dislodges during use, which renders the dilator component unusable, and can require the use of a replacement device.
Sold states
Worldwide - US Nationwide distribution in the states of PA, UT, FL, PA, OH, GA, MA, NV, CA, NY, NJ and the countries of UK, AU, TR, FR, CH, NO.
Affected count
490
Manufactured in
2220 Merritt Dr, N/A, Garland, TX, United States
Products
Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1968-2023Don't want to check this manually?
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