# FDA recall Z-0720-2023

> **Cordis US Corp** · Class II · device recall initiated 2022-11-07.

## Product

Cordis Angiographic Catheter Extensions.      Used to transport fluid from the power injector to the catheter for injection into the patient.

## Reason for recall

There is a potential for separation at the male connector.

## Distribution

Nationwide distribution to AZ, CA, DC, FL, GA, KY, LA, MD, MS, NY, OH, TX, WV, WY and PR.  International distribution to Japan, Korea, Republic of, United Arab Emirates, Austria, Belgium, Czech Republic, Germany, Spain, France, United Kingdom, Iceland, Ireland, Israel, Netherlands, Portugal, Russia.

## Key facts

- **Recall number:** Z-0720-2023
- **Recalling firm:** Cordis US Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-07
- **Report date:** 2022-12-21

- **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-0720-2023

## Citation

> AI Analytics. FDA recall Z-0720-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0720-2023. Source: US FDA. Licensed CC0.

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