# FDA recall Z-2544-2020

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2020-06-04.

## Product

Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts. The Cardinal Health NPWT PRO family of systems provides care in the acute, extended and home care settings.

## Reason for recall

Canisters potentially contain an oversized O-ring that  cannot be installed into the mating connector on the device.

## Distribution

Worldwide distribution - US Nationwide distribution and the country of Canada.

## Key facts

- **Recall number:** Z-2544-2020
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-04
- **Report date:** 2020-07-15
- **Termination date:** 2025-08-05

- **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-2544-2020

## Citation

> AI Analytics. FDA recall Z-2544-2020. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2544-2020. Source: US FDA. Licensed CC0.

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