Becton Dickinson & Company BD Vacutainer Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer Push Button Blood Collection Set with the needle protector removed prior to needle retraction. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Vacutainer Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer Push Button Blood Collection Set with the needle protector removed prior to needle retraction.
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot / Serial Number. 9079767 9079770 9081829 9086811 9086812 9091607 9091626 9094659 9094661 9098547 9100711 9100712 9115965 9115913
Becton Dickinson & Company is recalling BD Vacutainer Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Pr due to Separation of front and rear barrels upon activation of the safety feature that retracts the needle. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Separation of front and rear barrels upon activation of the safety feature that retracts the needle
Recommended Action
Per FDA guidance
1. Immediately review your inventory for Catalog# 368656 with the lot numbers listed. Return all product subject to recall according to the Packing Instructions enclosed. 2. Identify all your customers that purchased affected lots of Catalog #368656, as listed . E-mail an excel file listing of all customers with their email addresses to BD6086@stericycle.com, within 72 hours of receipt of this letter so that BD may notify these customers directly. 3. Complete the attached Distributor Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material so that BD may acknowledge your receipt of this notification and process your credit accordingly. Please note that this is in addition to providing the customer list For any question please contact Customer/Technical Support: 888-237-2762 OPT 3, OPT 2; Monday Friday 8:00am - 5:00pm (CT)
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