---
title: "SeaSpine Polyaxial Head REF Number: 41-3010 — FDA record Z-2762-2026 | Is It on Recall"
description: "Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion."
url: https://isitonrecall.com/recall/fda-device-z-2762-2026-seaspine-polyaxial-head-ref-number-41-3010/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SeaSpine Polyaxial Head REF Number: 41-3010 — FDA record Z-2762-2026

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 May 28, 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**: SeaSpine Polyaxial Head REF Number: 41-3010
- **Reason**: Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
- **Classification**: Class II
- **Recalling firm**: SEASPINE ORTHOPEDICS CORPORATION
- **Quantity**: 796 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2762-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2762-2026%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 | UDI: 10889981155117; Affected Lots: AW199682G, AW199684G. |

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

## Distribution

Worldwide - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, Connecticut, Florida, Illinois, Indiana, Kansas, Maryland, Michigan, Missouri, Mississippi, Montana, Nevada, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, and Wyoming. The countries of Chile and Australia.

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

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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 29, 2026
- **Recall initiation date**: May 28, 2026
- **Center classification date**: Jul 20, 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-2762-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [SEASPINE ORTHOPEDICS CORPORATION records](https://isitonrecall.com/brand/seaspine-orthopedics-corporation/)