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BioPro, Inc. recalls K-Wire Sterile Single Trochar .045, Item Number 19108 - Product Usage: Accessories to the BioPro Go-Ez screw system and
Recalled August 21, 2019 · FDA recall Z-2241-2019 · BioPro
Hazard
Manufacturing flaw in the sterile barrier system · FDA Class II
Units
1 unit
Sold at
Worldwide distribution - US Nationwide distribution in the states of FL, LA, MD, NC, NY, OR & TX, and countries of Ecuador, Scotland.
Description
Manufacturing flaw in the sterile barrier system
Product
K-Wire Sterile Single Trochar .045, Item Number 19108 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Manufacturer(s)
BioPro, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →