--- title: "Capio SLIM Suture Capturing Device, Box of 5, Outer Package UPN: M0068318261,... — FDA record Z-2451-2024 | Is It on Recall" description: "Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention." url: https://isitonrecall.com/recall/fda-device-z-2451-2024-capio-slim-suture-capturing-device-box-of-5-outer-package-upn-m0068318261-inner-package-upn-m0068318/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Capio SLIM Suture Capturing Device, Box of 5, Outer Package UPN: M0068318261, Inner Package UPN: M0068318260. Capio S... — FDA record Z-2451-2024 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Jun 27, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Capio SLIM Suture Capturing Device, Box of 5, Outer Package UPN: M0068318261, Inner Package UPN: M0068318260. Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical procedures. - **Reason**: Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention. - **Classification**: Class II - **Recalling firm**: Boston Scientific Corporation - **Quantity**: 70,890 units total - **Agency-reported status**: Ongoing - **Source record identifier**: Z-2451-2024 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2451-2024%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | UPN: M0068318261 (Pack of 5), M0068318260 (Individual Pack); UDI/DI: 08714729842224 (Pack of 5), 08714729842804 (Individual Pack); Lot Numbers: 30110296, 30110298, 30254839, 30269668, 30277679, 30340398, 30348745, 30361515, 30369786, 30477997, 30485719, 30502470, 30509859, 30566414, 30571306, 30579075, 30594738, 30597768, 30601523, 30601525, 30608273, 30621482, 30622202, 30628533, 30642670, 30671135, 30825890, 30834186, 30849605, 30853891, 30862718, 30870581, 30877151, 30880729, 31248068, 31305827, 31316815, 31324676, 31400076, 31442842, 31459986, 31475463, 31479225, 31488049, 31494812, 31502318, 31509747, 31514250, 31583783, 31592632, 31600746, 31609045, 31621292, 31764817, 31779852, 31791062, 31809880, 31821132, 31866608, 31876830, 31876835, 31876837, 32040502, 32057254, 32146583, 32163271, 32230325, 32238124, 32351364, 32361264, 32370219, 32385442, 32400087, 32409539, 32418519, 32420869, 32447685, 32456405, 32465857, 32478780, 32499939, 32515625, 32518619, 32526697, 32829992, 32915635, 32979863, 32998255, 33008248, 33017302, 33065907, 33069479, 33216295, 33236632, 33259078, 33283648, 33311001, 33319579, 33375040, 33383769, 33394221, 33404930, 33422407, 33424886, 33454127, 33479450, 33530347, 33556283, 33564420, 33618759, 33670919, 33676308, 33815834 | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Domestic: Nationwide Distribution. International: Pending States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2451-2024%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Boston Scientific Corporation records](https://isitonrecall.com/brand/boston-scientific-corporation/)