Recalls from BD SWITZERLAND SARL

• BD Alaris Pump Infusion Sets (opens in a new tab)
  High risk, FDA, Sep 15, 2026, Device defect
• BD Intravascular Administration and Extension Sets (opens in a new tab)
  Moderate risk, FDA, Aug 13, 2026, Sterility problem
• BD Medline 111 Gravity Set (opens in a new tab)
  Moderate risk, FDA, Jul 2, 2026, Unapproved product
• BD Connecta Stopcocks (opens in a new tab)
  Moderate risk, FDA, Jun 18, 2026, Device defect

Data: Recall Canary (opens in a new tab)