Boston Scientific Corporation recalls Capio SLIM Box 5, Model #M0068318261; Intended for use in general suturing applications during open surgery to assist i…
- Recall date
- February 12, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1617-2018
- FDA classification
- Class II
- Brand / firm
- Boston Scientific Corporation
- Sold / distributed
- Worldwide Distribution -- US, Brazil, Guatemala, Ecuador, Malaysia, Czech Republic, United Kingdom, Argentina, Honduras, Peru, Singapore, Denmark, Iceland, Chile, Nicaragua, Venezuela, Japan, Egypt, Israel, Canada, Panama, Taiwan, United Arab Emirates, Finland, Ireland, Mexico, Dominican Republic,…
Why it was recalled
Potential for Capio sutures to break and /or detach.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Capio SLIM Box 5, Model #M0068318261; Intended for use in general suturing applications during open surgery to assist in the placement of suture material in tissues at the operative site.
Get recall alerts
Free email alert whenever Boston Scientific Corporation has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Boston Scientific Corporation