Bard Access Systems, Inc. Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual Driver Needle Kit 15mm x 15Ga, D015251NK/ BD Needle Kit for Powered Driver 25mm x 15Ga, D015251MK/ BD Manual Driver Needle Kit 25mm x 15Ga, D015351NK/ BD Needle Kit for Powered Driver 35mm x 15Ga, D015351MK/ BD Manual Driver Needle Kit 35mm x 15Ga, D015451NK/ BD Needle Kit for Powered Driver 45mm x 15Ga, D015451MK/ BD Manual Driver Needle Kit 45mm x 15Ga, D015551 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual Driver Needle Kit 15mm x 15Ga, D015251NK/ BD Needle Kit for Powered Driver 25mm x 15Ga, D015251MK/ BD Manual Driver Needle Kit 25mm x 15Ga, D015351NK/ BD Needle Kit for Powered Driver 35mm x 15Ga, D015351MK/ BD Manual Driver Needle Kit 35mm x 15Ga, D015451NK/ BD Needle Kit for Powered Driver 45mm x 15Ga, D015451MK/ BD Manual Driver Needle Kit 45mm x 15Ga, D015551
Brand
Bard Access Systems, Inc.
Lot Codes / Batch Numbers
Catalog/UDI/Lot: D015151NK/801741163586/, 121460, 122145, 123307, 125298, 125534, 125662, 126095, 126467, 126677, 127040, 127711, 128002, 128208, 128778, D015151MK/801741163623/122359, D015251NK/801741163678/121496, 122096, 123306, 125299, 125533, 125535, 126075, 126149, 126178, 126569, 126686, 127118, 127170, 127417, 127756, 128001, 128482, 128829, D015251MK/801741163630/122193, D015351NK/801741163593/125721, 126901, 126939, 128385, D015351MK/801741163647/125842, D015451NK/801741163609/121593, 122169, 123305, 125016, 125517, 125770, 125977, 126299, 126300, 126340, 126575, 127092, 127119, 127300, 127516, 127808, 128120, 128487, 128725, D015451MK/801741163654/122375, 123433, D015551NK/801741163616/125841, 126951, 127003, 127496, 128724, D015551MK/801741163661/125843, 126834, D001001/00801741163579/All Lots
Products Sold
Catalog/UDI/Lot: D015151NK/801741163586/, 121460, 122145, 123307, 125298, 125534, 125662, 126095, 126467, 126677, 127040, 127711, 128002, 128208, 128778; D015151MK/801741163623/122359; D015251NK/801741163678/121496, 122096, 123306, 125299, 125533, 125535, 126075, 126149, 126178, 126569, 126686, 127118, 127170, 127417, 127756, 128001; 128482, 128829; D015251MK/801741163630/122193; D015351NK/801741163593/125721, 126901, 126939, 128385; D015351MK/801741163647/125842; D015451NK/801741163609/121593, 122169, 123305, 125016, 125517, 125770, 125977, 126299, 126300, 126340, 126575, 127092, 127119, 127300, 127516, 127808, 128120, 128487, 128725; D015451MK/801741163654/122375, 123433; D015551NK/801741163616/125841, 126951, 127003, 127496, 128724; D015551MK/801741163661/125843, 126834; D001001/00801741163579/All Lots
Bard Access Systems, Inc. is recalling Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver due to BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss of intraosseous access; 2) Stylet safety mechanism may not engage as the stylet is removed; 3) Metal discs in the powered driver may stick rendering the driver unusable.
Recommended Action
Per FDA guidance
On 06/20/22 BD mailed or emailed recall notices to customers asking them to: 1)Quarantine all affected devices. Destroy needle kits and keep intraosseous drivers quarantined until they can be inspected and repaired, if required, by firm sales representatives. 2) Share this notice with all users within your facility and network and with any organization where the potentially affected products have been transferred. 3) There is no replacement product at this time. The firm will notify customers when replacement products are available. 4) If you purchased affected product from a distributor, contact this distributor for further instructions. 5) If you purchased products directly, complete and return the response form. 6) Distributors were asked to identify all customers within their distribution network that purchased any affected product and to provide a copy of the customer letter. Recall Notice: https://bdx.force.com/CC360/s/impactedproducts?language=en_US&id=7018a000001Gn1tAAC Customers requiring further assistance can contact the North American Regional Complaint Center 1-844-823-5433, say "Recall" when prompted, Mon-Fri 8:00AM-5:00PM CT or productcomplaints@bd.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026