---
title: "LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - D... — FDA record Z-0421-2023 | Is It on Recall"
description: "Potential for intraoperative screw head separation at weld location."
url: https://isitonrecall.com/recall/fda-device-z-0421-2023-linesider-spinal-system-pedicle-screws-5-5-6-0mm-non-mod-standard-7-1mm-dual-lead-non-cannulated-mod/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number L... — FDA record Z-0421-2023

Reported terminated

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 Aug 3, 2022. 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**: LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number LS-N6SG6545. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped individually, as tray replenishments. Used in spinal fixation surgery.
- **Reason**: Potential for intraoperative screw head separation at weld location.
- **Classification**: Class II
- **Recalling firm**: Integrity Implants Inc.
- **Quantity**: 50 screws
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0421-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2023%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 | Part/Model Number LS-N6SG6545; UDI: (01)00818613027815(10)10210067; Lot Number: 10210067 |

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

## Distribution

US distribution to California, Indiana, New York, Oklahoma, Washington DC

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

- [California](https://isitonrecall.com/state/california/)
- [District of Columbia](https://isitonrecall.com/state/district-of-columbia/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Dec 14, 2022
- **Recall initiation date**: Aug 3, 2022
- **Center classification date**: Dec 5, 2022
- **Termination date**: Oct 23, 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-0421-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Integrity Implants Inc. records](https://isitonrecall.com/brand/integrity-implants-inc/)