---
title: "Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150. — FDA record Z-2833-2026 | Is It on Recall"
description: "Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization."
url: https://isitonrecall.com/recall/fda-device-z-2833-2026-stryker-hoffmann-ii-connecting-rod-micro-3-x-150mm-catalog-number-50796150/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150. — FDA record Z-2833-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 1, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.
- **Reason**: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- **Classification**: Class II
- **Recalling firm**: Stryker GmbH
- **Quantity**: 5,664 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2833-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2833-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog Number: 50796150. GTIN: 04546540389954. All lot numbers. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, ID, IL, KS, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, PA, RI, SC, TN, TX, VA, WI, WV and the countries of Australia, Austria, Belgium, Canada, Chile, Denmark, France, Germany, Greece, Ireland, Israel, Italy, Japan, Kuwait, Netherlands, Poland, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, UK.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Aug 5, 2026
- **Recall initiation date**: Jul 1, 2026
- **Center classification date**: Jul 29, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2833-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stryker GmbH records](https://isitonrecall.com/brand/stryker-gmbh/)
