---
title: "Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Icon... — FDA record Z-0518-2024 | Is It on Recall"
description: "Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inserter, when the inserters bend, it may als"
url: https://isitonrecall.com/recall/fda-device-z-0518-2024-iconix-knotless-1-4mm-anchor-with-xbraid-s-blue-black-ref-3911-714-520-iconix-knotless-1-4mm-anchor/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (... — FDA record Z-0518-2024

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 Oct 25, 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**: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand, wrist, elbow and shoulder.
- **Reason**: Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inserter, when the inserters bend, it may also move off the drill hole location leading to damage of the suture construct during insertion. Suture damage may lead to suture breaks during use.
- **Classification**: Class II
- **Recalling firm**: Riverpoint Medical, LLC
- **Quantity**: 999 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0518-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0518-2024%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 | Product Code: 3911-7 14-520 UDI-DI Code: 00840277402172 Lot Number: 23080433 Product Code: 3911-7 14-521 UDI-DI Code: 00840277402189 Lot Number: 23081617 |

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

## Distribution

U.S. Nationwide distribution in the state of CA.

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## Dates in the source

- **Report date**: Dec 20, 2023
- **Recall initiation date**: Oct 25, 2023
- **Center classification date**: Dec 8, 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-0518-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Riverpoint Medical, LLC records](https://isitonrecall.com/brand/riverpoint-medical-llc/)
