Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Recalled by Qapel Medical Inc. Due to Aspiration catheter distal tip features and characteristics may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Qapel Medical Inc. directly.
Affected Products
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including Cheetah Delivery Tool, REF: AP6072-132. 072 Aspiration Tubing, REF: APT-95
Quantity: 1617
Why Was This Recalled?
Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
Where Was This Sold?
This product was distributed to 29 states: AL, AZ, CA, CT, FL, GA, ID, IL, IN, LA, MA, MI, MN, MO, NE, NV, NJ, NY, NC, ND, OH, OK, PA, SC, SD, TN, TX, WA, WI
About Qapel Medical Inc.
Qapel Medical Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report