Stryker Instruments Div. of Stryker Corporation: Medical Device Recall in 2016 - (Recall #: Z-0584-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

Product Classification:

Class III

Date Initiated: October 11, 2016

Date Posted: November 23, 2016

Recall Number: Z-0584-2017

Event ID: 75485

Reason for Recall:

Stryker Instruments is voluntarily recalling the Care Instructions/Instructions for Use packaged with the Radiofrequency (RF) MultiGen¿ Generator, because the instructions for use incorrectly contained instructions supporting the sterilization of the MultiGen¿ cables.

Status: Terminated

Product Quantity: 2,675

Code Information:

RF MultiGen¿, 0406-900-000, Refurb RF MultiGen¿, 0406-900-000U

Distribution Pattern:

Domestic:AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY Foreign:France, Germany, Canada, UK, Lebanon, South Africa, Chile, Hong Kong, Poland, Argentina, Spain, Greece, Italy, India, Brazil, Switzerland, Netherlands, Sweden VA/DOD:

Voluntary or Mandated:

Voluntary: Firm initiated