Alaris Infusion Sets and BD Texium Syringes Recalled for Potential Drug Leaks

What You Should Do

1. The recalled products include various Alaris Pump Infusion Sets and BD Texium Needle-Free Syringes used for drug transfer and administration.
2. To determine if your supply is affected, check the Reference (REF) number, Unique Device Identifier (UDI), and lot numbers found on the individual product packaging. See the Affected Products section below for the full list of affected codes.
3. Stop using any recalled device immediately and separate them from your active inventory to prevent accidental use.
4. Contact BD Switzerland SARL or your medical device distributor to arrange for the return, replacement, or correction of the affected units.
5. If you have questions regarding this recall, contact BD at the information provided in the original notification letter or reach out to your local distributor.
6. For additional questions about medical device safety, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

Affected Products