# FDA recall Z-2033-2021

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2021-05-21.

## Product

Sterile Radial/Femoral Angiography Drape, Catalog Number 29529 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

## Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2033-2021
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-05-21
- **Report date:** 2021-07-14
- **Termination date:** 2024-01-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukegan, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2033-2021

## Citation

> AI Analytics. FDA recall Z-2033-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2033-2021. Source: US FDA. Licensed CC0.

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