Sonex Health recalls SX-One MicroKnives with potential dull blade that may affect surgical use. Affected units include specific part numbers and lot codes. Consumers should check their product details.
Potential of dull blade
Sonex Health is recalling SX-One MicroKnives due to a potential dull blade that could impact surgical effectiveness. This recall affects specific model numbers and production lots.
The microknife may become dull over time, reducing its effectiveness during surgical procedures. This could lead to incomplete tissue removal or require additional procedures.
Users of SX-One MicroKnives for medical procedures are affected. Healthcare professionals and medical facilities using the recalled models are most at risk.
Check for part number 600112-001 and lot codes listed in the recall notice. The product was sold with specific production dates and batch numbers.
Verify your SX-One MicroKnife's part number and lot codes against the list provided in the recall notice.
The recall is for potential dull blade that may affect surgical use, but it does not pose an immediate risk of injury.
Check for part number 600112-001 and lot codes listed in the recall notice.
The recall does not specify a remedy, so contact Sonex Health for further instructions.
We’ve drafted a message you can send Sonex Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1387-2022 — Sonex Health Sonex Health Hello, I own a Sonex Health that is covered by recall Z-1387-2022 from Sonex Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
