Reported May 16, 2018 · Terminated
Capio CL; Model #M0068311350. Indicated for the placement of suture in a variety of Transvaginal procedures.
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 CL; Model #M0068311350. Indicated for the placement of suture in a variety of Transvaginal procedures.
- Lot codes and dates
- UDI08714729516545
- Batch numbers
180112701824541119491588180112711865494119668541182299991888175919987267206027641917328620382965206027642085056921234964
- Amount recalled
- 1,258
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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