---
title: "Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, R... — FDA record Z-2934-2026 | Is It on Recall"
description: "The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a pro"
url: https://isitonrecall.com/recall/fda-device-z-2934-2026-endo-model-replacement-set-tibial-plateau-right-left-l-uhmwpe-cocrmo-rotating-hinge-item-number-15-0/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16 — FDA record Z-2934-2026

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 6, 2026. 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**: Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16
- **Reason**: The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.
- **Classification**: Class II
- **Recalling firm**: Waldemar Link GmbH & Co. KG (Mfg Site)
- **Quantity**: 1 US; 9 OUS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2934-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2934-2026%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 04026575432134 Lot for Implant REF 15-0027/16: 2604069 |

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

## Distribution

Domestic US distribution to Indiana. OUS distribution to Belarus and Germany.

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

- [Indiana](https://isitonrecall.com/state/indiana/)

## Dates in the source

- **Report date**: Aug 19, 2026
- **Recall initiation date**: Jul 6, 2026
- **Center classification date**: Aug 11, 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-2934-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Waldemar Link GmbH & Co. KG (Mfg Site) records](https://isitonrecall.com/brand/waldemar-link-gmbh-co-kg-mfg-site/)