FDA recall record

Revmedx XGAUZE Trauma Dressing, catalog number FIN-0002-01 recall — FDA Z-2762-2015

The XGAUZE Trauma Dressing was recalled because the packages may acquire small tears or pinholes during shipping due to use of shipping containers that…

Class IIclassification
Z-2762-2015official record ID
Sep 23, 2015report date

Recall record at a glance

Official recordZ-2762-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRevmedx Inc.
Report dateSep 23, 2015
Recall initiation dateAug 12, 2015
Quantity5004 units
LocationWilsonville, OR, United States

Official product description

XGAUZE Trauma Dressing, catalog number FIN-0002-01. XGAUZE is a 3" x 36" z-folded rayon/polyester dressing embedded with individual compressed cellulose sponges. Upon contact with blood or exudate, the sponges expand, thus increasing the dressing's capacity to absorb fluids. XGAUZE is packed in a pre-formed sterile barrier system (pouch sealed on three sides); one side is a PET/foil/PE film, and the other side is a PET/aluminum oxide/PE film. Packages are vacuum sealed and terminally sterilized via gamma radiation.

Why the product was recalled

The XGAUZE Trauma Dressing was recalled because the packages may acquire small tears or pinholes during shipping due to use of shipping containers that lacked adequate protective materials. If present, these small tears or pinholes may disrupt package integrity and render the device unsterile.

Distribution information

US Distribution to the states of : Arizona, Idaho, North Carolina, Tennessee and Virginia.

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: Telephone.

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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