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U.S. Department of Health and Human Services

Class 1 Device Recall BD Intraosseous Needle Sets, BD Intraosseous Manual Driver Kit and BD Intraosseous Powered Driver

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  Class 1 Device Recall BD Intraosseous Needle Sets, BD Intraosseous Manual Driver Kit and BD Intraosseous Powered Driver see related information
Date Initiated by Firm June 20, 2022
Date Posted July 22, 2022
Recall Status1 Open3, Classified
Recall Number Z-1397-2022
Recall Event ID 90315
510(K)Number K203193  K191976  
Product Classification Needle, hypodermic, single lumen - Product Code FMI
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,
D015551NK/ BD Needle Kit for Powered Driver 55mm x 15Ga,
D015551MK/ BD Manual Driver Needle Kit 55mm x 15G,
D001001/ BD Intraosseous Powered Driver (drill)
Code Information 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
Recalling Firm/
Manufacturer		 Bard Access Systems, Inc.
605 N 5600 W
Salt Lake City UT 84116-3738
For Additional Information Contact
801-522-5000
Manufacturer Reason
for Recall		 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.
FDA Determined
Cause 2		 Process change control
Action 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
Quantity in Commerce 40,734
Distribution Distribution US nationwide and Canada.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = FMI and Original Applicant = Bard Access Systems, Inc(BAS)[Wholly-owned subsidiary of BD]
510(K)s with Product Code = FMI and Original Applicant = Piper Access, LLC
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