---
title: "Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Ca... — FDA record Z-2357-2024 | Is It on Recall"
description: "Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces."
url: https://isitonrecall.com/recall/fda-device-z-2357-2024-brand-name-meridian-angled-awl-fixed-product-name-angled-awl-fixed-model-catalog-number-ra2-003015-p/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Descrip... — FDA record Z-2357-2024

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 Jun 4, 2024. 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**: Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No
- **Reason**: Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
- **Classification**: Class II
- **Recalling firm**: SEASPINE ORTHOPEDICS CORPORATION
- **Quantity**: 100 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2357-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2357-2024%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 | Lot Code: UDI 10889981216368 Lot Numbers TT0190H, TT0191H |

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

## Distribution

The product was distributed to the following US states: Nevada, Colorado, Texas, Washington, Indiana, Georgia, Michigan, Florida, Pennsylvania, Illinois, Tennessee, Virginia, Missouri, South Dakota, California, Montana, Minnesota, Arizona

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Montana](https://isitonrecall.com/state/montana/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Jul 24, 2024
- **Recall initiation date**: Jun 4, 2024
- **Center classification date**: Jul 15, 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-2357-2024%22)

## Related records

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