Intuitive Surgical recalls Da Vinci X/Xi clip appliers (models 470230, 470327, 470401) due to potential for unexpected motion from partial disengagement. Affected units may need replacement.
Due to the potential for unexpected motion caused by the partial disengagement of the instrument from the system.
Intuitive Surgical is recalling Da Vinci X/Xi surgical clip appliers because they might detach from the system during use, causing unexpected movement. This could lead to injury if the instrument moves unexpectedly during surgery.
The clip appliers might partially disengage from the surgical system during use, causing unexpected movement. This could lead to unintended instrument motion that might harm the patient or surgical team.
Surgical teams using Da Vinci X/Xi systems with the recalled clip appliers are most at risk. Patients and staff during surgery could be affected if the instrument moves unexpectedly.
Check for the model numbers 470230, 470327, or 470401 on the clip appliers. All units sold with Da Vinci X/Xi systems are affected.
Look for model numbers 470230, 470327, or 470401 on the clip appliers.
Reach out to Intuitive Surgical for guidance on next steps if you have the recalled models.
The recall is due to the potential for unexpected motion caused by partial disengagement of the instrument from the system.
Da Vinci X/Xi Large Clip Applier (model 470230), Medium-Large Clip Applier (model 470327), and Small Clip Applier (model 470401).
No, but you should check if you have the recalled models and contact Intuitive Surgical for guidance.
We’ve drafted a message you can send Intuitive Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1460-2022 — Intuitive Surgical Intuitive Surgical Hello, I own a Intuitive Surgical that is covered by recall Z-1460-2022 from Intuitive Surgical. 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.
