Recall archive / 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. Source coverage and dates.
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
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.
| 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 |
Announcement retrieved Oct 1, 2026. Official announcement.
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.