FDA recall record

vyaire Flexible Patient Circuit, 3100A, REF 29028-003, intended to be used with the 3100A recall — FDA Z-0488-2024

Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were…

Class IIclassification
Z-0488-2024official record ID
Dec 13, 2023report date

Recall record at a glance

Official recordZ-0488-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmVyaire Medical
Report dateDec 13, 2023
Recall initiation dateOct 27, 2023
Quantity188 circuits
LocationMettawa, IL, United States

Official product description

vyaire Flexible Patient Circuit, 3100A, REF 29028-003, intended to be used with the 3100A High Frequency Oscillatory Ventilator (HFOV)

Why the product was recalled

Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were distributed in the U.S.

Distribution information

US: Florida

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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