Reported Dec 18, 2025 · Announced
Olympus Corporation recalls Olympus Single use ligating device due to PolyLoop device may fail to detach as expected and become anchored to patient anatomy
Olympus Corporation
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.What you should do
Stop using the product and follow the return or refund instructions in the firm's announcement.
Is this the product you have?
- Single use ligating device BrandOlympus. Medical Devices
Why it was recalled
PolyLoop device may fail to detach as expected and become anchored to patient anatomy
The agency has not ranked the risk yet — treat the notice as a caution.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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