Reported Apr 16, 2025 · Ongoing

Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072…

Qapel Medical Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Qapel Medical Inc. · 4245 Technology Dr · Fremont, CA · 94538-6339

Is this the product you have?

  • Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing
  • REFAPT6072-132. Hippo 072 Aspiration System including Cheetah Delivery Tool
  • REFAP6072-132. 072 Aspiration Tubing
  • REFAPT-95
Lot codes and dates
  • REF/UDI-DI/Lot(Expiration)APT6072-132/00857545008127/FG241008C-03(04/07/2025), FG240916C-04(03/17/2025), FG240905C-04(03/06/2025). AP6072-132/00857545008097/FG241206A-03(06/08/2025), FG240917A-01(03/17/2025). APT-95/00857545008103/FG241206A-04(06/08/25)
Amount recalled
1617

Where it was sold

Why it was recalled

Stop using this product now

Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.