FDAOctober 11, 2016device
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Terminated
Brands named
stryker instruments divstrykerstryker instruments
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDABW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
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