FDA recall record

Resmed Quattro Air FFM MED  AMER, Product Code: 62702, full face mask for use with recall — FDA Z-2550-2016

Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.

Class IIclassification
Z-2550-2016official record ID
Aug 24, 2016report date

Recall record at a glance

Official recordZ-2550-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmResmed Corporation
Report dateAug 24, 2016
Recall initiation dateJul 12, 2016
Quantity42 units
LocationSan Diego, CA, United States

Official product description

Quattro Air FFM MED  AMER, Product Code: 62702, full face mask for use with active-exhaust-valve ventilators

Why the product was recalled

Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.

Distribution information

US nationwide distribution

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: Letter.

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

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