# FDA recall Z-1512-2025

> **Qapel Medical Inc.** · Class I · device recall initiated 2025-02-26.

## Product

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

## Reason for recall

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

## Distribution

US: CA, IL, NE, TN, TX, NJ, NC, SD, FL, MI, PA, GA, AL, IN, NY, WI, AZ, MN, LA, OH, OK, SC, NV, ND, ID, MO, CT, WA, MA.  OUS: QATAR, United Arab Emirates, Republic of Kazakhstan

## Key facts

- **Recall number:** Z-1512-2025
- **Recalling firm:** Qapel Medical Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-26
- **Report date:** 2025-04-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fremont, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1512-2025

## Citation

> AI Analytics. FDA recall Z-1512-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1512-2025. Source: US FDA. Licensed CC0.

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