---
title: "stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side:... — FDA record Z-1651-2025 | Is It on Recall"
description: "A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking. \" Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow co"
url: https://isitonrecall.com/recall/fda-device-z-1651-2025-stryker-latitude-ev-humeral-revision-stem-trial-l-150mm-size-large-side-right-ref-9030103-prosthesis/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, ... — FDA record Z-1651-2025

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 Mar 3, 2025. 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 Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented
- **Reason**: A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking. " Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow color indicator (incorrect) " Device Actually: 9030092, Humeral Stem Trial 150mm Medium / Left, Red color indicator (correct)
- **Classification**: Class II
- **Recalling firm**: Tornier, Inc
- **Quantity**: 5 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1651-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1651-2025%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 | GTIN 00846832015054, Batch Number CC0421265 |

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

## Distribution

OUS (International) Distribution to countries: Sweden, Australia, United Kingdom, Colombia, Germany

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Apr 30, 2025
- **Recall initiation date**: Mar 3, 2025
- **Center classification date**: Apr 22, 2025

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-1651-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Tornier, Inc records](https://isitonrecall.com/brand/tornier-inc/)