# FDA recall Z-2461-2026

> **Howmedica Osteonics Corp.** · Class II · device recall initiated 2026-05-19.

## Product

TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.

## Reason for recall

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).

## Distribution

US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.

## Key facts

- **Recall number:** Z-2461-2026
- **Recalling firm:** Howmedica Osteonics Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-19
- **Report date:** 2026-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2461-2026

## Citation

> MORVS. FDA recall Z-2461-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2461-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*