---
title: "BD: Intraosseous Vascular Access System Needle Sets — FDA announcement Aug 3, 2026 | Is It on Recall"
description: "Due to Reports of Difficulty Removing the Obturator"
url: https://isitonrecall.com/recall/fdapress-fa7b821ecd1d41bb-bd-intraosseous-vascular-access-system-needle-sets/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# BD: Intraosseous Vascular Access System Needle Sets — FDA announcement Aug 3, 2026

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Aug 3, 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**: Intraosseous Vascular Access System Needle Sets
- **Reason**: Due to Reports of Difficulty Removing the Obturator
- **Classification**: Not supplied
- **Recalling firm**: (Becton, Dickinson and Company)
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: fa7b821ecd1d41bb

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | BD will issue replacement for destroyed product of the affected lot numbers to customers that purchased the affected product directly from BD, following receipt of the completed Customer Response Form.; Product Name \| Catalog No. \| Lot No. \| UDI-DI \| Expiration Date \| Product Package Size; Needle Kit for Powered Driver 15mm x 15Ga \| D015151NK \| See Appendix 1 in customer letter\* \| 00801741163586 \| See Appendix 1 in customer letter\* \| 6 kits per case; Needle Kit for Powered Driver 25mm x 15Ga \| D015251NK \| 00801741163678; Needle Kit for Powered Driver 35mm x 15Ga \| D015351NK \| 00801741163593; Needle Kit for Powered Driver 45mm x 15Ga \| D015451NK \| 00801741163609; Needle Kit for Powered Driver 55mm x 15Ga \| D015551NK \| 00801741163616 |

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

## Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

**FDA company announcement, table 1**

| Product Name | Catalog No. | Lot No. | UDI-DI | Expiration Date | Product Package Size |
| --- | --- | --- | --- | --- | --- |
| Needle Kit for Powered Driver 15mm x 15Ga | D015151NK | See Appendix 1 in customer letter\* | 00801741163586 | See Appendix 1 in customer letter\* | 6 kits per case |
| Needle Kit for Powered Driver 25mm x 15Ga | D015251NK | See Appendix 1 in customer letter\* | 00801741163678 | See Appendix 1 in customer letter\* | 6 kits per case |
| Needle Kit for Powered Driver 35mm x 15Ga | D015351NK | See Appendix 1 in customer letter\* | 00801741163593 | See Appendix 1 in customer letter\* | 6 kits per case |
| Needle Kit for Powered Driver 45mm x 15Ga | D015451NK | See Appendix 1 in customer letter\* | 00801741163609 | See Appendix 1 in customer letter\* | 6 kits per case |
| Needle Kit for Powered Driver 55mm x 15Ga | D015551NK | See Appendix 1 in customer letter\* | 00801741163616 | See Appendix 1 in customer letter\* | 6 kits per case |

Announcement retrieved Oct 1, 2026. [Official announcement](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due).

## Distribution

Not supplied

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

## Dates in the source

- **Fda listing date**: Aug 3, 2026
- **Company announcement date**: Jul 30, 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://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Becton, Dickinson and Company records](https://isitonrecall.com/brand/becton-dickinson-and-company/)