FDA Device recall Z-0584-2017
RF MultiGen¿, 0406-900-000
- FDA Device
- Class III
- terminated
- Published 2016-11-23
On 2016-11-23 the FDA classified a Class III recall of RF MultiGen¿, 0406-900-000 by Stryker Instruments Div, citing stryker Instruments is voluntarily recalling the Care Instructions/Instructions for Use packaged with the Radiofrequency (RF) MultiGen¿ Generator, because the instructions for use….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0584-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-10-11 |
| Published | 2016-11-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Instruments Div |
| Distribution | 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 |
Product
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Reason
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.
Identifiers
| code_info | RF MultiGen¿, 0406-900-000, Refurb RF MultiGen¿, 0406-900-000U |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0584-2017%22
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