FDA recall record

Intuitive Surgical Ion Endoluminal System, REF: 380748-65 recall — FDA Z-2720-2024

There is a potential that the robotic system's instrument cart arm may contain screws that may potentially fail which could result in uncontrolled motion…

Class IIclassification
Z-2720-2024official record ID
Sep 4, 2024report date

Recall record at a glance

Official recordZ-2720-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmIntuitive Surgical, Inc.
Report dateSep 4, 2024
Recall initiation dateJul 12, 2024
Quantity3 units
LocationSunnyvale, CA, United States

Official product description

Ion Endoluminal System, REF: 380748-65

Why the product was recalled

There is a potential that the robotic system's instrument cart arm may contain screws that may potentially fail which could result in uncontrolled motion of a catheter inside a patient's airways.

Distribution information

US Nationwide distribution in the states of AZ and CA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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