---
title: "Grafton DBM Putty, Model Numbers: a) T43102, b) T43102INT, c) T43103INT, d) T... — FDA record Z-0167-2024 | Is It on Recall"
description: "Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed acc"
url: https://isitonrecall.com/recall/fda-device-z-0167-2024-grafton-dbm-putty-model-numbers-a-t43102-b-t43102int-c-t43103int-d-t43105-e-t43105int-f-t43110-g-t43/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Grafton DBM Putty, Model Numbers: a) T43102, b) T43102INT, c) T43103INT, d) T43105, e) T43105INT, f) T43110, g) T4311... — FDA record Z-0167-2024

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 Sep 26, 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**: Grafton DBM Putty, Model Numbers: a) T43102, b) T43102INT, c) T43103INT, d) T43105, e) T43105INT, f) T43110, g) T43110INT; Demineralized Bone Matrix
- **Reason**: Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
- **Classification**: Class II
- **Recalling firm**: Medtronic Sofamor Danek USA Inc
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0167-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0167-2024%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 | a) T43102: b) T43102INT: c) T43103INT: d) T43105: e) T43105INT: f) T43110: g) T43110INT: |

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

## Distribution

US, Colombia, S. Korea, New Zealand, India, Taiwan

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Nov 1, 2023
- **Recall initiation date**: Sep 26, 2023
- **Center classification date**: Oct 24, 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-0167-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Sofamor Danek USA Inc records](https://isitonrecall.com/brand/medtronic-sofamor-danek-usa-inc/)