Boston Scientific recalls Capio SLIM Suture Capturing Devices with specific lot numbers due to inconsistent suture capture, potentially requiring additional medical procedures during surgery.
Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
Boston Scientific is recalling certain Capio SLIM Suture Capturing Devices because some units may not consistently catch sutures after activation. This could lead to longer surgeries or extra medical steps for patients.
The device may not consistently capture sutures after activation, which could cause the procedure to take longer than expected. This might require additional medical steps to secure the suture properly, increasing surgical time and potential complications.
Physicians using the Capio SLIM Suture Capturing Devices during open surgical procedures are most affected. Patients undergoing surgery with these devices may face extended procedures or additional interventions.
Check the lot numbers listed in the recall: 29729168, 29729169, 29972338, 30110291, and other specific numbers provided in the recall notice. The product is sold as a 1-Pack of Capio SLIM Suture Capturing Devices.
Look for the lot number on the device packaging or label to determine if it is in the recalled list.
Reach out to Boston Scientific directly for further assistance or to confirm if your device is affected.
Boston Scientific recalls certain Capio SLIM Suture Capturing Devices because some lots do not consistently catch sutures after activation, which could lead to longer procedures or additional medical interventions.
The affected lot numbers include 29729168, 29729169, 29972338, 30110291, and other specific numbers listed in the recall notice.
No, the recall does not require immediate discontinuation. Physicians should check the lot number and contact Boston Scientific if they have the affected device.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2452-2024 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-2452-2024 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.
