Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN Recalled by Boston Scientific Corporation Due to Packaging Incomplete Seal. Users noted an incomplete pouch...
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 Boston Scientific Corporation directly.
Affected Products
Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670; M00562672 (Box 20), M00562670; M00562673 (Box 40), M00562670; M00562691 (Box 5); M00562690; M00562692 (Box 20), M00562690; M00562693 (Box 40), M00562690.
Quantity: 335,788 units total (Domestic: 222,882, Foreign: 112,906)
Why Was This Recalled?
Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Boston Scientific Corporation
Boston Scientific Corporation has 601 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report