RF MultiGen¿ — Class III medical device recall Z-0584-2017
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2016-11-23, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Stryker Instruments is voluntarily recalling the Care Instructions/Instructions for Use packaged with the Radi
| Recall number | Z-0584-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2016-10-11 |
| Classified | 2016-11-16 |
| Reported by FDA | 2016-11-23 |
| Terminated | 2017-07-25 |
| Distributed | 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 |
| Countries outside the US | AR, BR, CA, CH, CL, DE, ES, FR, GB, GR, HK, IN, IT, LB, NL, PL, SE, ZA |
| Quantity | 2,675 |
| Model numbers | 0406-900-000U |
Product
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0584-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.