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BD® PhaSeal™ System

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BD PhaSeal™ System

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Alert

Important Update: BD® PhaSeal™ System and SmartSite™ VialShield Closed Vial Access Device Discontinuation


NOTE: This does NOT pertain to the BD® PhaSeal™ Optima Closed System Transfer Devices (CSTD)

Learn what this means for your facility and explore next steps below.

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Why are the PhaSeal™ System and SmartSite™ VialShield devices being discontinued?

After careful consideration and in alignment with the BD commitment to innovation and safety, we have made the decision to retire the original PhaSeal™ Closed System Transfer Devices (CSTD) and the SmartSite™ VialShield Vial Access Devices.  Based on current production schedules, we anticipate that inventory of the discontinued PhaSeal™ and SmartSite™ VialShield codes in the United States will be depleted by July 1, 2026. 

Once inventory is depleted, we are confident that the BD® PhaSeal™ Optima System will continue to meet your hazardous drug preparation and administration safety needs.

Transitioning to PhaSeal™ Optima

Instruments

PhaSeal™ Optima: The Next Generation

BD has pioneered the CSTD category by listening to healthcare professionals who handle hazardous drugs every day. The PhaSeal™ Optima System builds on the proven foundation of the original PhaSeal™ System, maintaining its core architecture and physical barrier technology to prevent exposure. This includes a vapor-capturing mechanism in the vial protector and membrane-to-membrane connections that self-seal upon disconnect, ensuring airtight, leakproof transfers.

Learn more

Discontinuation Timeline


            

Announcement
February 2026
Transition to Optima
February 1, 2026 - July 1, 2026
Last order date
July 1, 2026
Final support date
October 1, 2026

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BD PhaSeal™ System
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Reference

*Within an ISO Class V environment following aseptic technique 

†The ability to prevent microbial ingress for up to 168 hours should not be interpreted as modifying, extending, or superseding a manufacturer’s labeling recommendations for the storage and expiration dating of the drug vial. Refer to the drug manufacturer’s recommendations and USP compounding guidelines for shelf life and sterility information.

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Resources
EIFUs
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