---
title: "LITe Decompression Snake Arm, REF 48080230 — FDA record Z-0610-2024 | Is It on Recall"
description: "Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft."
url: https://isitonrecall.com/recall/fda-device-z-0610-2024-lite-decompression-snake-arm-ref-48080230/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# LITe Decompression Snake Arm, REF 48080230 — FDA record Z-0610-2024

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 1, 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**: LITe Decompression Snake Arm, REF 48080230
- **Reason**: Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
- **Classification**: Class II
- **Recalling firm**: Stryker Spine
- **Quantity**: 9
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0610-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0610-2024%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 (GTIN): 07613327263909, lot # 227764. |

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

## Distribution

US: MD, MI, NM, TX & OUS: Canada & France.

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

- [Maryland](https://isitonrecall.com/state/maryland/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [New Mexico](https://isitonrecall.com/state/new-mexico/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Dec 27, 2023
- **Recall initiation date**: Nov 1, 2023
- **Center classification date**: Dec 21, 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-0610-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stryker Spine records](https://isitonrecall.com/brand/stryker-spine/)