# FDA recall Z-2463-2023

> **Stryker Corporation** · Class II · device recall initiated 2023-07-10.

## Product

SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the manual process of counting, displaying and recording the number of RFID-tagged absorbent articles used during surgical procedures  Product Code: 0694-002-090;

## Reason for recall

Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2463-2023
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-10
- **Report date:** 2023-09-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2463-2023

## Citation

> AI Analytics. FDA recall Z-2463-2023. Retrieved 2026-07-31 from https://api.ai-analytics.org/recall/Z-2463-2023. Source: US FDA. Licensed CC0.

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