QLT USA, Inc. Atrisorb FreeFlow Bioabsorbable Guided Tissue Regeneration (GTR) Barrier, Sterile Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Atrisorb FreeFlow Bioabsorbable Guided Tissue Regeneration (GTR) Barrier, Sterile
Brand
QLT USA, Inc.
Lot Codes / Batch Numbers
Lot 2072A, Exp 5/2007
Products Sold
Lot 2072A, Exp 5/2007
QLT USA, Inc. is recalling Atrisorb FreeFlow Bioabsorbable Guided Tissue Regeneration (GTR) Barrier, Sterile due to Injectable needles were included in procedure kits instead of sterile blunt cannulas.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Injectable needles were included in procedure kits instead of sterile blunt cannulas.
Recommended Action
Per FDA guidance
Consignee was notified by letter on 1/26/2006.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
PA
Page updated: Jan 10, 2026