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FDA (Device enforcement)Recalled 2021-01-19class ii

Boston Scientific Corporation: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M005

Is my product affected?

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 (Bo

  • UPC 08714729283904
  • UPC 08714729747598
  • UPC 08714729283928
  • UPC 08714729747611
  • UPC 08714729158110
  • UPC 08714729748069
  • UPC 08714729268802
  • UPC 08714729158141
  • UPC 08714729748083
  • UPC 08714729268819
  • UPC 08714729501664
  • UPC 08714729158158
  • UPC 08714729748106
  • UPC 08714729268826
  • UPC 08714729501671

Check against the official notice below — it lists the full affected range.

What happened

Boston Scientific Corporation is recalling Captivator, Captiflex, and Sensation Short Throw Single-Use Polypectomy Snares due to incomplete seals on the inner pouches of the devices. Users identified incomplete pouch seals before using the devices on patients. The recall affects 335,788 units distributed nationwide in the United States, with specific lot and batch numbers identified across multiple product configurations and GTINs.

The recall record does not specify a remedy for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

Details from the source

Reason for recall: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient. Distribution: US nationwide distribution. Quantity: 335,788 units total (Domestic: 222,882, Foreign: 112,906) Lot/code info: Outer box GTIN: 08714729283904 Inner pouch GTIN: 08714729747598 Lot/Batch#: 24818278, 24906823, 25042455 Outer box GTIN: 08714729283928 Inner pouch GTIN: 08714729747611 Lot/Batch#: 24685766, 24817145, 24899710, 24739786, 25006735, 24861901 Outer box GTIN: 08714729158110 Inner pouch GTIN: 08714729748069 Lot/Batch#: 24685764, 24890051, 24824132 Outer box GTIN: 08714729268802 Inner pouch GTIN: 08714729748069 Lot/Batch#: 25023345 Outer box GTIN: 08714729158141 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24699718, 24939626, 24861739 Outer box GTIN: 08714729268819 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24824134, 25006729, 24709534 Outer box GTIN: 08714729501664 Inner pouch GTIN: 08714729748083 Lot/Batch#: 25023203, 24697822, 24739587, 24942292, 24909214, 24824136 Outer box GTIN: 08714729158158 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24856636, 24927642, 24699218 Outer box GTIN: 08714729268826 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24835709, 24818605, 25023343 Outer box GTIN: 08714729501671 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24909216, 24758832, 24872119, 24994171, 25048397, 2475126, 24929431, 24995438

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

Related recalls

All FDA (Device enforcement) recalls

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