---
title: "Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws lab... — FDA record Z-0846-2024 | Is It on Recall"
description: "Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length were manufactured using an incorrect screw shank component, and so the labeling is incorrect bec"
url: https://isitonrecall.com/recall/fda-device-z-0846-2024-cortera-spinal-fixation-system-ref-150100-85050-spinal-fixation-screws-labeled-as-8-5-mm-diameter-50/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length. — FDA record Z-0846-2024

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 Nov 28, 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**: Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length.
- **Reason**: Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length were manufactured using an incorrect screw shank component, and so the labeling is incorrect because the affected screws are in fact 5.5 diameter, 45 mm length screws, which if used may lead to the screw not engaging.
- **Classification**: Class II
- **Recalling firm**: XTANT Medical Holdings, Inc
- **Quantity**: 6
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0846-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0846-2024%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: 00810076564005, Lot: AP23000143 |

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

## Distribution

US distribution in MI.

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

- [Michigan](https://isitonrecall.com/state/michigan/)

## Dates in the source

- **Report date**: Feb 7, 2024
- **Recall initiation date**: Nov 28, 2023
- **Center classification date**: Jan 29, 2024

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-0846-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [XTANT Medical Holdings, Inc records](https://isitonrecall.com/brand/xtant-medical-holdings-inc/)