Qapel Medical recalls Hippo 072 Aspiration System with Cheetah Delivery Tool and Aspiration Tubing due to potential tip detachment, vessel rupture, and vasospasm from FDA clearance issues.
Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
Qapel Medical is recalling its Hippo 072 Aspiration System, including the Cheetah Delivery Tool and Aspiration Tubing, because the catheter tip may detach, causing vessel rupture or vasospasm. This could lead to serious medical complications if used improperly.
The aspiration catheter's distal tip may not meet FDA clearance standards, which could cause it to detach during use. This detachment might lead to vessel rupture or vasospasm (narrowing of blood vessels), potentially causing serious medical complications.
Healthcare professionals using the Hippo 072 Aspiration System for medical procedures are most at risk. Patients undergoing procedures with this system could experience complications if the catheter tip detaches.
Check for the product name 'Hippo 072 Aspiration System' with the reference numbers APT6072-132 or AP6072-132. The tubing has reference numbers like APT-95 and specific expiration dates.
Identify the product by checking the reference numbers on the packaging, such as APT6072-132 or AP6072-132.
Reach out to Qapel Medical for guidance on whether the product is affected and what steps to take next.
The recall indicates potential risks, so it is not recommended for use until the manufacturer provides guidance.
Contact Qapel Medical directly to determine if your specific product is affected and follow their instructions.
Look for reference numbers like APT6072-132 or AP6072-132 on the packaging, and check the expiration dates listed on the tubing.
We’ve drafted a message you can send Qapel Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1512-2025 — Qapel Medical Qapel Medical Hello, I own a Qapel Medical that is covered by recall Z-1512-2025 from Qapel Medical. 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.
