ClearanceBrief
Recall Z-3179-2026 ยท FMI Needle, Hypodermic, Single Lumen

embecta Medical II LLC

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100

DateSep 16, 2026 (initiated Jul 26, 2023)
StatusOpen, Classified
ReasonRetrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.
Root causeNonconforming Material/Component
ActionOn July 26, 2023, Embecta Medical II LLC ( subsidiary of Becton, Dickinson and Company 'BD's) issued a recall notification to consignees via email. Embecta ask consignees to take the following actions: 1. Immediately review your inventory for the specific Catalog (Ref) numbers listed above. If it is labeled with a "For investigational Use Only" statement, discard the product. 2. Share this advisory notification with anyone in your facility/office who may have received the product to ensure they are also aware of this advisory. 3. Identify all patients that may have received the affected
Quantity4300 Final Count (in EA)
DistributionUS Nationwide distribution in the states of MA, KY, CT, TX, NJ, OH, MN, LA, IN, NH, AL, CA, NY, FL, NC, MI, SC, AZ, VA, GA, PA, MO.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K212015BD Nano 2nd Gen Pen Needle
Becton, Dickinson and Company, Nov 19, 2021