Reported May 16, 2018 · Terminated
Capio SLIM Suture Capturing Device, Model #M0068318250. Intended for use in general suturing applications during open…
Boston Scientific Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Boston Scientific Corporation · 100 Boston Scientific Way · Marlborough, MA · 01752-1234
Is this the product you have?
- Capio SLIM Suture Capturing Device, Model #M0068318250. Intended for use in general suturing applications during open surgery to assist in the placement of suture material in tissues at the operative site.
- Lot codes and dates
- UDI08714729842224
- Batch numbers
81 of 81 codes
177812061933546320312941177828081943507820423794177903161956815820453711177924691957347520453712179863211970115120475301179916961971151120484084181064071983397320484085181102531985868320532136182135701985895020628943183040521988206620633409183841081988206720637817184079741988727920693087184206871994284420697608184924941995978120838671184947371996349220838674186204811999329720838675187402382000079620838676187921842000116020902944188552592000116120968694189224882000675721065530
- Amount recalled
- 21,250
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
Why it was recalled
Potential for Capio sutures to break and /or detach.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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