# FDA recall Z-2035-2020

> **Applied Medical Resources Corp** · Class II · device recall initiated 2020-01-31.

## Product

STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

## Reason for recall

Failure of cardiovascular clips to provide sufficient occlusion of the vessel.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KY, MA, MI, MO, NC, NE, NJ, NY, OK, PA, TN, TX, UT, VA. WA and WI. The countries of Austria, Australia, Canada, Switzerland, Germany, Spain, Finland, France, Italy, Japan, Mexico, and Netherlands.

## Key facts

- **Recall number:** Z-2035-2020
- **Recalling firm:** Applied Medical Resources Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-31
- **Report date:** 2020-05-27
- **Termination date:** 2022-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rancho Santa Margarita, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2035-2020

## Citation

> AI Analytics. FDA recall Z-2035-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2035-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*