FDADecember 11, 2020device

VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

UPCs

00085412531274

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →