BD Needle Kit for Powered Driver 15mm x 15Ga — Class I medical device recall Z-2872-2026
Ongoing recall by Bard Access Systems, Inc., reported 2026-08-26, distributed in AL, AR, AZ, CA, CO, FL, GA, IA…. After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to o
| Recall number | Z-2872-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Access Systems, Inc., Salt Lake City, UT, United States |
| Recall initiated | 2026-07-30 |
| Classified | 2026-08-14 |
| Reported by FDA | 2026-08-26 |
| Distributed | AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA |
| Quantity | 80,200 |
| UPC / GTIN / UDI-DI | 00801741163586, 00801741163593, 00801741163609, 00801741163616, 00801741163678 |
| Model numbers | D015151NK, D015251NK, D015351NK, D015451NK, D015551NK |
Product
BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle Kit for Powered Driver 35mm x 15Ga, REF: D015351NK, BD Needle Kit for Powered Driver 45mm x 15Ga, REF: D015451NK, BD Needle Kit for Powered Driver 55mm x 15Ga, REF: D015551NK
Reason for recall
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2872-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.