Boston Scientific recalls Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor due to difficulty tracking over guidewire, potentially causing procedural delays.
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
Boston Scientific is recalling a specific ureteral stent set because it may cause problems tracking the guidewire during procedures, which could lead to delays needing device exchange. This affects medical professionals using the product in urological procedures.
The stent set may cause difficulty or inability to track over the guidewire during procedures. This could lead to procedural delays as the healthcare team may need to exchange the affected device.
Medical professionals who use the Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor during urological procedures are most at risk. The recall applies to specific lot numbers and model.
Check for the model 'Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor' and lot number 24795838. The product was sold with UPN: M006175262110.
Verify the model number and lot number to confirm if your stent set is affected.
The recall is for potential procedural delays due to difficulty tracking the guidewire, not an immediate safety hazard.
Check the model and lot number to see if it's affected; the recall does not require immediate action but may need device exchange if issues occur.
Look for the model 'Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor' and lot number 24795838.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1733-2020 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1733-2020 from Boston Scientific. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
