# FDA recall Z-0960-2019

> **Abbott Vascular** · Class II · device recall initiated 2018-07-03.

## Product

PLUS 30 PRIORITY PACK Accessory Kit    Product Usage:  Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).

## Reason for recall

Incorrect expiration being entered for one lot.

## Distribution

US Nationwide Distribution - NC and NY

## Key facts

- **Recall number:** Z-0960-2019
- **Recalling firm:** Abbott Vascular
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-03
- **Report date:** 2019-03-06

- **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-0960-2019

## Citation

> AI Analytics. FDA recall Z-0960-2019. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-0960-2019. Source: US FDA. Licensed CC0.

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