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Stryker Instruments Div. of Stryker Corporation recalls EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter tip
Recalled June 3, 2015 · FDA recall Z-1671-2015 · Stryker Instruments Div. of Stryker
Hazard
Potential for the device cannula to overthrow past the intended length. · FDA Class II
Units
1,420 Units
Sold at
US Nationwide Distribution including AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NJ, NM, NV, NY, OK, OR, PA, TN, TX, UT, VA, and WI.
Description
Potential for the device cannula to overthrow past the intended length.
Product
EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter tip, and 10 cm with and without HiLiter tip.
Manufacturer(s)
Stryker Instruments Div. of Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →