ProductGuru Recalls

Official recall record

BD Bodyguard Microset

Health Canada — Medical Devices · 2024-03-06 · CanadaType I
Issuing authority
Health Canada — Medical Devices
Published
2024-03-06
Country of alert
Canada
Alert level
Type I
Alert type
recall

What the authority reported

BD received customers complaints, that the new clamp on the y-port of the BD Bodyguard™ Microset (clamp supplied since 2021) can be opened more easily compared to the clamp which was used before 2021. Patients may accidentally lay on the infusion set and unintentionally open the clamp causing the infusion set to be exposed to atmospheric air/ environment, if a vented clamp is being used. The longer this failure mode remains undetected the higher the potential volume of air entry. Recall start date: February 26, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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