Intuitive Surgical recalls da Vinci SP surgical systems (models SP0022-SP0026) due to potential cannula mount button damage when released abruptly. Affected systems may require repair or replacement.
The firm became aware of a problem with the surgical system where the cannula mount button may be damaged when the user releases the button abruptly.
Intuitive Surgical is recalling specific models of their da Vinci SP surgical systems because the cannula mount button can be damaged if released abruptly. This could affect how surgeons position surgical tools during procedures.
The cannula mount button may become damaged when released abruptly, potentially affecting the surgical system's ability to position instruments and cameras. This could lead to improper tool placement during procedures.
Surgeons and surgical teams using the affected da Vinci SP models (SP0022-SP0026) are most at risk. These systems are used in operating rooms for minimally invasive surgery.
Check if your da Vinci SP surgical system has model numbers SP0022, SP0023, SP0024, SP0025, or SP0026. The Patient Cart (PC) is the component that supports surgical tools and cameras.
Identify the model number on your da Vinci SP system to confirm if it is affected (SP0022-SP0026).
The affected models are SP0022, SP0023, SP0024, SP0025, and SP0026.
The firm became aware that the cannula mount button may be damaged when released abruptly, potentially affecting surgical tool positioning.
No, the recall does not require immediate stop use. Affected systems can continue to be used with caution.
We’ve drafted a message you can send Intuitive Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0845-2020 — Intuitive Surgical Intuitive Surgical Hello, I own a Intuitive Surgical that is covered by recall Z-0845-2020 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.
