Reported Apr 29, 2020 · Ongoing
Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor UPN: M006175262110
Boston Scientific
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 · 100 Boston Scientific Way · Marlborough, MA · 01752-1234
Is this the product you have?
- Percuflex Plus Ureteral Stent Set 6FX24CM with .038
- Sensor UPNM006175262110
- Lot codes and dates
- Lot Numbers24795838
- Amount recalled
- 91 units
This recall covers 12 products
The agency filed one notice per product. You are reading one of them; the other 11 are below.
Where it was sold
- Nationwide
Why it was recalled
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device
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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