# FDA recall Z-0957-2019

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2018-12-27.

## Product

Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm)  Product Code: 8044 - Product Usage: Ideal for applying ointments, prepping, wiping needles, cleaning slides and more   Rayon/polyester blend construction   Highly absorbent.

## Reason for recall

Curity All Purpose Sponges were not sterilized and distributed

## Distribution

Worldwide distribution - US Nationwide and countries of  Canada, Colombia.

## Key facts

- **Recall number:** Z-0957-2019
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-12-27
- **Report date:** 2019-03-06
- **Termination date:** 2020-06-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0957-2019

## Citation

> AI Analytics. FDA recall Z-0957-2019. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-0957-2019. Source: US FDA. Licensed CC0.

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