---
title: "Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00... — FDA record Z-1567-2022 | Is It on Recall"
description: "An incorrect sizing label was applied to the carton packaging."
url: https://isitonrecall.com/recall/fda-device-z-1567-2022-stryker-swanson-flexspan-finger-joint-implant-w-o-grommets-silicone-size-00-ref-4700020-sterile/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile. — FDA record Z-1567-2022

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 27, 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 SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
- **Reason**: An incorrect sizing label was applied to the carton packaging.
- **Classification**: Class II
- **Recalling firm**: Wright Medical Technology, Inc.
- **Quantity**: 17 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1567-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1567-2022%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 numbers 1728375 and 1728376, UDI #00840420121707. |

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

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, NY, PA, and TN. The countries of the Australia, France, the Netherlands, Sweden, and the United Kingdom.

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 31, 2022
- **Recall initiation date**: Jul 27, 2022
- **Center classification date**: Aug 23, 2022

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-1567-2022%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/)
