ClearanceBrief
Recall Z-2451-2024 ยท PWI Instrumentation, Surgical Mesh, Urogynecologic, Transvaginal Repair Of Pelvic Organ Prolapse

Boston Scientific Corporation

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.

DateJul 30, 2024 (initiated Jun 27, 2024)
StatusOpen, Classified
ReasonSome lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
Root causeProcess change control
ActionOn June 27, 2024 URGENT MEDICAL DEVICE REMOVAL - IMMEDIATE ACTION REQUIRED letters were sent to consignees. Actions to be taken: This removal affects only the products listed in Attachment 1 (Affected Products). No other material numbers or lots are impacted by this removal. Further distribution or use of any remaining product affected by this removal should cease immediately. For Capio SLIM devices that were successfully used in a procedure, no action is needed. Affected worldwide regulatory authorities are being notified of this removal as required. Immediately post this information in a vis
Quantity70,890 units total
DistributionDomestic: Nationwide Distribution. International: Pending
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K172060Capio SLIM Suture Capturing Device
Boston Scientific Corporation, Nov 3, 2017