# FDA recall Z-2473-2021

> **Cypress Medical Products LLC** · Class II · device recall initiated 2021-08-11.

## Product

McKesson Lap Sponge, X-Ray Detectable 	12"x 12", 5/pack, Sterile McKesson Part #	16-2112121

## Reason for recall

Manufacturer issued a recall due to an EO indicator color. The indicator should change from red to blue signifying sterilization. However, on one case of product, the indicators did not change

## Distribution

VA

## Key facts

- **Recall number:** Z-2473-2021
- **Recalling firm:** Cypress Medical Products LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-11
- **Report date:** 2021-09-22
- **Termination date:** 2023-07-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2473-2021

## Citation

> AI Analytics. FDA recall Z-2473-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2473-2021. Source: US FDA. Licensed CC0.

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