---
title: "Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla... — FDA record Z-1184-2024 | Is It on Recall"
description: "Holding arm could move (twist) uncontrollably in the front area. This could lead to a serious deterioration of patient's safety if the movement is transferred t"
url: https://isitonrecall.com/recall/fda-device-z-1184-2024-rebstock-holding-rod-for-fixation-for-holding-and-fixation-of-flexible-leyla-arms-and-spatula-art-no/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla Arms and spatula Art. No. 06-06-285 and... — FDA record Z-1184-2024

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 Dec 21, 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**: Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla Arms and spatula Art. No. 06-06-285 and 06-06-285MOD. surgical instrument.
- **Reason**: Holding arm could move (twist) uncontrollably in the front area. This could lead to a serious deterioration of patient's safety if the movement is transferred to the spatula, which is attached to the holding arm.
- **Classification**: Class II
- **Recalling firm**: Medagent Inc
- **Quantity**: 84 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1184-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1184-2024%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 | Batches: 6221672, 6222079, 6230282, 6230985, 6230986, 6231808, 6222559, 6231989, 6221673 |

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

## Distribution

TX Foreign: Algeria China Dominican Republic Germany India Japan Philippines UK

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

- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Mar 6, 2024
- **Recall initiation date**: Dec 21, 2023
- **Center classification date**: Feb 23, 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-1184-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medagent Inc records](https://isitonrecall.com/brand/medagent-inc/)