Reported May 22, 2013 · Terminated

DuraGen XS Dural Regeneration Matrix DuraGen XS Dural Regenerative Matrix is an absorbable implant for repair of dural…

Integra LifeSciences Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Integra LifeSciences Corporation · 105 Morgan Ln · Plainsboro, NJ · 08536-3339

Is this the product you have?

  • DuraGen XS Dural Regeneration Matrix DuraGen XS Dural Regenerative Matrix is an absorbable implant for repair of dural defects. DuraGen XS is an easy to handle, soft, white, pliable, non-friable, porous collagen matrix. DuraGen XS is supplied sterile, non-pyrogenic, for single use in double peel packages in a variety of sizes.
Lot codes and dates
    • 1125963
    • 1130387 1130386
    • 1130468
Amount recalled
52 boxes

This recall covers 21 products

The agency filed one notice per product. You are reading one of them; the other 20 are below.

8 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 3, 2015 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.