Bd Switzerland Sarl recalls

All Bd Switzerland Sarl recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (11).

11 recalls published between April 9, 2025 and September 23, 2026. Most common issues: sterility (6). 1 was FDA Class I, the most serious level.

• BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD… recall
  FDA September 23, 2026 · Bd Switzerland Sarl · Class I
• 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code:… recall
  FDA August 19, 2026 · Bd Switzerland Sarl · Class II
• MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites recall
  FDA July 8, 2026 · Bd Switzerland Sarl · Class II
• BD Connecta" BD Luer-Lok" 360 recall
  FDA June 24, 2026 · Bd Switzerland Sarl · Class II
• BD PhaSeal Injector Luer (N30C) recall
  FDA September 3, 2025 · Bd Switzerland Sarl · Class II
• BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD Texium: 3 mL recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD Texium Needle-Free Syringe: 3 mL recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium… recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD Connecta BD Luer-Lok 360 recall
  FDA April 9, 2025 · Bd Switzerland Sarl · Class II