---
title: "REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair , — FDA record Z-1612-2023 | Is It on Recall"
description: "Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged."
url: https://isitonrecall.com/recall/fda-device-z-1612-2023-ref-5065-kendall-impad-rigid-sole-foot-cover-regular-pair/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair , — FDA record Z-1612-2023

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 Apr 14, 2023. 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 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,
- **Reason**: Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged.
- **Classification**: Class II
- **Recalling firm**: Stryker Sustainability Solutions
- **Quantity**: 50 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1612-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1612-2023%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 # 0000157564, UDI-DI: 00885825013585 |

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

## Distribution

US: WA OUS: None

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

- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: May 24, 2023
- **Recall initiation date**: Apr 14, 2023
- **Center classification date**: May 19, 2023

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-1612-2023%22)

## Related records

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