Conavi Medical recalls Novasight Hybrid Catheter model TA-06-0001 due to potential sheath detachment. Affected units may cause injury during medical procedures.
Due to manufacturing issues there is a potential for the catheter sheath to detach.
Conavi Medical is recalling Novasight Hybrid Catheter model TA-06-0001 because of a potential manufacturing issue that could cause the catheter sheath to detach during use. This could lead to injury if the sheath separates while being used in medical procedures.
The catheter sheath may detach due to manufacturing issues, which could cause injury during medical procedures. This is a potential risk when the catheter is used for real-time ultrasound and optical imaging in adults.
Medical professionals using the Novasight Hybrid Catheter for diagnostic imaging procedures are most at risk. Patients receiving the procedure may also be affected if the catheter sheath detaches.
Check for the model number TA-06-0001 on the packaging. The catheter is a 3Fr single-use sterile device used for diagnostic imaging. It was sold with specific expiration dates and lot numbers listed in the recall notice.
Look for the model number TA-06-0001 on the packaging or product label.
Reach out to Conavi Medical for further assistance or to confirm if your unit is affected.
The recall states there is a potential for the catheter sheath to detach due to manufacturing issues, so it is not recommended for use until the recall is addressed.
Check the model number on the packaging. If it matches TA-06-0001, contact Conavi Medical for guidance on next steps.
The recall lists specific expiration dates (2024-06 to 2025-06) and lot numbers. Check the packaging for these details.
We’ve drafted a message you can send Novasight to request your refund or repair — edit it as you like.
Subject: Recall Z-1585-2025 — Novasight Novasight Hello, I own a Novasight that is covered by recall Z-1585-2025 from Novasight. 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.
