Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing steps from those stated in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Intuitive Surgical, Inc. directly.
Affected Products
8MM,MEDIUM-LARGE CLIP APPLIER ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
Quantity: 509 total units, all affected devices
Why Was This Recalled?
Deviations in reprocessing steps from those stated in the reprocessing instructions can cause surface degradation of the housing and/or accelerate mechanical wear of the instrument.
Where Was This Sold?
This product was distributed to 8 states: FL, IN, MA, NV, NY, OR, TX, UT
About Intuitive Surgical, Inc.
Intuitive Surgical, Inc. has 244 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report