---
title: "REF: 5921-018-135, Stryker Color Cuff, 18\" (Red), Quick Connect Single Port, ... — FDA record Z-0664-2022 | Is It on Recall"
description: "Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder inflatable cuffs."
url: https://isitonrecall.com/recall/fda-device-z-0664-2022-ref-5921-018-135-stryker-color-cuff-18-red-quick-connect-single-port-single-bladder/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder — FDA record Z-0664-2022

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 Jan 21, 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**: REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder
- **Reason**: Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder inflatable cuffs.
- **Classification**: Class II
- **Recalling firm**: Stryker Sustainability Solutions
- **Quantity**: 40 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0664-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0664-2022%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 # 12983349 |

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

## Distribution

US: KS OK TX OUS: None

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

- [Kansas](https://isitonrecall.com/state/kansas/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Mar 2, 2022
- **Recall initiation date**: Jan 21, 2022
- **Center classification date**: Feb 22, 2022
- **Termination date**: Feb 26, 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-0664-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stryker Sustainability Solutions records](https://isitonrecall.com/brand/stryker-sustainability-solutions/)