# FDA recall Z-0250-2020

> **Cordis Corporation** · Class II · device recall initiated 2019-10-04.

## Product

Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.

## Reason for recall

Product was manufactured utilizing an expired inner body.

## Distribution

US distribution to AL, AZ, FL, MN, and MO

## Key facts

- **Recall number:** Z-0250-2020
- **Recalling firm:** Cordis Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-04
- **Report date:** 2019-11-06
- **Termination date:** 2020-12-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami Lakes, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0250-2020

## Citation

> AI Analytics. FDA recall Z-0250-2020. Retrieved 2026-07-30 from https://api.ai-analytics.org/recall/Z-0250-2020. Source: US FDA. Licensed CC0.

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