---
title: "AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (... — FDA record Z-1067-2024 | Is It on Recall"
description: "Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues."
url: https://isitonrecall.com/recall/fda-device-z-1067-2024-aft-allograft-filler-tube-diverted-tube-3-4-filled-product-code-227005-bone-void-filler/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler) — FDA record Z-1067-2024

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 22, 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**: AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
- **Reason**: Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
- **Classification**: Class II
- **Recalling firm**: Musculoskeletal Transplant Foundation, Inc.
- **Quantity**: 50
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1067-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1067-2024%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 | UDI-DI: W4184227005T0473 Donor Lots 00322029241137 and 00322039641144 |

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

## Distribution

Product was distributed to Minnesota.

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

- [Minnesota](https://isitonrecall.com/state/minnesota/)

## Dates in the source

- **Report date**: Feb 21, 2024
- **Recall initiation date**: Dec 22, 2023
- **Center classification date**: Feb 9, 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-1067-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Musculoskeletal Transplant Foundation, Inc. records](https://isitonrecall.com/brand/musculoskeletal-transplant-foundation-inc/)