# FDA recall Z-2370-2020

> **Abbott Vascular** · Class II · device recall initiated 2020-03-25.

## Product

Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus Content: 209 ¿g; Lot number 903224A,

## Reason for recall

Incorrect expiration date

## Distribution

US Nationwide distribution including in the states of NJ, HI, MD, FL, NV, CA, KS and PR. No foreign consignee

## Key facts

- **Recall number:** Z-2370-2020
- **Recalling firm:** Abbott Vascular
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-25
- **Report date:** 2020-06-24
- **Termination date:** 2021-07-12

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2370-2020

## Citation

> AI Analytics. FDA recall Z-2370-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2370-2020. Source: US FDA. Licensed CC0.

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