Official recall notice

FDA DeviceClass INotable

FDA Recall: Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

Recall date
2026-05-13
FDA class
Class I

Why it was recalled

Hazard

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Recommended action

What to do

75 kits

Product description

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Verify with the official notice →
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