---
title: "Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component o... — FDA record Z-1735-2022 | Is It on Recall"
description: "Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an"
url: https://isitonrecall.com/recall/fda-device-z-1735-2022-stryker-usb-converter-polaris-spectra-camera-catalog-201148-a-component-of-the-mako-robotic-arm-assi/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery ... — FDA record Z-1735-2022

Reported terminated

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 Aug 8, 2022. 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 USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.
- **Reason**: Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
- **Classification**: Class II
- **Recalling firm**: Mako Surgical Corporation
- **Quantity**: 2
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1735-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1735-2022%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 | Lot #22041607, UDI-DI (GTIN) 07613327407280. |

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

## Distribution

US Distribution was made to IL and AZ.

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Illinois](https://isitonrecall.com/state/illinois/)

## Dates in the source

- **Report date**: Sep 21, 2022
- **Recall initiation date**: Aug 8, 2022
- **Center classification date**: Sep 9, 2022
- **Termination date**: May 22, 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-1735-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mako Surgical Corporation records](https://isitonrecall.com/brand/mako-surgical-corporation/)