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RecallsAboutBlog

BD Switzerland Sarl

BD Switzerland Sarl: 4 recalls listed since June 2026 across FDA; 1 rated high risk.

By year

  • 20264

By agency

  • FDA4

By category

  • Medical Device4

All recalls (4)

BD Alaris Pump Infusion Sets

BD Alaris Pump Infusion Sets have performance data discrepancies that may lead to inappropriate pump performance.

High risk, FDA, , Device defect

BD Intravascular Administration and Extension Sets

Intravascular administration sets may not have received adequate sterilization processing.

Moderate risk, FDA, , Sterility problem

BD Medline 111 Gravity Set

The gravity set was shipped as an engineering sample labeled not for human use.

Moderate risk, FDA, , Unapproved product

BD Connecta Stopcocks

BD Connecta BD Luer-Lok 360 Stopcocks may have an unstable connection at Port C when used with a plastic luer-lok syringe.

Moderate risk, FDA, , Device defect
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