Intuitive Surgical Recalls 8mm Micro Bipolar Forceps Due to Reprocessing Deviations
Intuitive Surgical is recalling 509 units of 8mm Micro Bipolar Forceps because deviations in reprocessing steps can cause surface degradation and mechanical wear.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any hospitalizations, injuries, or illnesses. The hazard is related to potential mechanical wear and surface degradation due to reprocessing deviations, which fits the criteria for a moderate severity recall without reported harm.
Plain-English summary
Intuitive Surgical, Inc. is recalling 509 units of 8mm Micro Bipolar Forceps. These instruments are intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments. The affected units are identified by part number 470171-05 and are all 8mm da Vinci Xi (IS4000) Surgical System instruments manufactured with white colored housings.
The recall was initiated because 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. The affected units were distributed in Florida, Texas, New York, Nevada, Oregon, Indiana, Utah, and Massachusetts.
Healthcare facilities should stop using the affected instruments and contact Intuitive Surgical for further instructions. Consumers are not directly affected by this recall as the product is intended for professional medical use.
The recalled product
- Product
- 8MM,MICRO BIPOLAR FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
- Manufacturer
- Intuitive Surgical, Inc.
- Affected units
- 509
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Part number: 470171-05
Distribution
Part of a larger recall action
This product is one of 22 recalled by Intuitive Surgical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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