# FDA recall Z-0811-2020

> **Howmedica Osteonics Corp.** · Class II · device recall initiated 2019-11-07.

## Product

Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum   Catalog #:  2041C-3254

## Reason for recall

May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire

## Distribution

CA, FL, GA , IA, MA, MI, NC, OH, WI  Foreign: Canada, Japan

## Key facts

- **Recall number:** Z-0811-2020
- **Recalling firm:** Howmedica Osteonics Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-07
- **Report date:** 2020-01-22
- **Termination date:** 2020-08-31

- **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-0811-2020

## Citation

> AI Analytics. FDA recall Z-0811-2020. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-0811-2020. Source: US FDA. Licensed CC0.

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