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Stryker Instruments Div. of Stryker Corporation recalls Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is u
Recalled May 17, 2017 · FDA recall Z-2071-2017 · Stryker Instruments Div. of Stryker
Hazard
Product shipped proximate to or past the expiration date listed on the product label. · FDA Class II
Units
65
Sold at
US (nationwide) Distribution to the states of : CA, CT, GA, IL, IN, MA, MD, NC, OH, PA, TN, and TX.
Description
Product shipped proximate to or past the expiration date listed on the product label.
Product
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.
Manufacturer(s)
Stryker Instruments Div. of Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →