---
title: "Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02; — FDA record Z-1513-2026 | Is It on Recall"
description: "The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture."
url: https://isitonrecall.com/recall/fda-device-z-1513-2026-endo-model-sl-connection-component-incl-pe-plateau-item-number-16-2840-02/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02; — FDA record Z-1513-2026

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 Jan 12, 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 SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
- **Reason**: The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- **Classification**: Class II
- **Recalling firm**: Waldemar Link GmbH & Co. KG (Mfg Site)
- **Quantity**: 49 units (OUS only)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1513-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1513-2026%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 | Item Number: 16-2840/02; UDI-DI: 04026575359233; Serial/Lot Number: 250925/0640 , 250925/0641, 250925/0642, 250925/0646, 250925/0650, 250925/0652, 250925/0653 , 250925/0656, 250925/0658, 250925/0669, 250925/0670, 250925/0680, 250925/0681 , 250925/0682, 250925/0687, 250925/0689, 250925/0690, 250925/0691, 250925/0693 , 250925/0694, 251110/3293, 250925/0660, 250925/0661, 250925/0684, 250925/0685 , 250925/0657, 250925/0663, 250925/0659, 250925/0678, 251110/3288, 251110/3292 , 251110/3303, 251110/3313, 250925/0683, 250925/0674, 250925/0644, 250925/0665 , 250925/0668, 250925/0671, 250925/0673, 250925/0676, 250925/0664 , 250925/0651 , 251110/3297, 251110/3289, 250925/0639, 250925/0648, 250925/0688, 250925/0696; |

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

## Distribution

Worldwide - US Nationwide distribution in the state of NJ and the countries of Belarus, Canada, Switzerland , Colombia, Germany, Spain, United Kingdom, Hungary, India, Italy, Netherlands, Romania, Saudi Arabia.

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**: Mar 18, 2026
- **Recall initiation date**: Jan 12, 2026
- **Center classification date**: Mar 10, 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-1513-2026%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/)
