---
title: "stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty — FDA record Z-1477-2024 | Is It on Recall"
description: "Stryker has identified an issue that impacts specific lots of Infinity\" Resection Guide Adjustment Blocks. The parts within these three lots were found to have"
url: https://isitonrecall.com/recall/fda-device-z-1477-2024-stryker-infinity-resection-adjustment-block-ref-33600030-ankle-arthroplasty/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty — FDA record Z-1477-2024

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 6, 2024. 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 Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
- **Reason**: Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.
- **Classification**: Class II
- **Recalling firm**: Wright Medical Technology, Inc.
- **Quantity**: 47 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1477-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1477-2024%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 | UDI/DI 00889797004008, Lot Numbers: 2656950, 2762126, 2796094 |

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

## Distribution

US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE, GERMANY, ITALY, SPAIN, SWEDEN, SWITZERLAND, UK

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

- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Apr 10, 2024
- **Recall initiation date**: Mar 6, 2024
- **Center classification date**: Apr 4, 2024

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-1477-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Wright Medical Technology Inc records](https://isitonrecall.com/brand/wright-medical-technology-inc/)