FDA Device Intelligence
HomeBOSTON SCIENTIFIC CORPORATION › Capio SLIM

Capio SLIM

BOSTON SCIENTIFIC CORPORATION · Model M0068318250 · UDI-DI 08714729838005

PWI Prescription
2
510(k) clearances
239
Adverse events
13
Recalls
8
Facilities

Description

Suture Capturing Device

Recalls

DateFirmReason
2024-06-27Boston Scientific CorporationSome lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
2024-06-27Boston Scientific CorporationSome lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific Corporation
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.
2018-02-12Boston Scientific CorporationPotential for Capio sutures to break and /or detach.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.