Capio RP M0068321010Recalls & reported problems
Boston Scientific Corporation · Suture Capturing Device · Class 1
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Feb 12, 2018Terminated
Potential for Capio sutures to break and /or detach.
Z-1621-2018 · Root cause: Device Design · FDA record ↗
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- NA 26173HAKarl Storz GmbH & Co. KG · HOLDER, NEEDLE, GASTROENTEROLOGIC3 reports
- Integra® Jarit® 121210Integra Lifesciences Production Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC2 reports
- V. Mueller RH2551Steris Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC1 report
- Integra® Jarit® 120135Integra Lifesciences Production Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.