Integra LifeSciences Corp Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm) , Sterile; Integra LifeSciences Corporation, 311 Enterprise Drive, Plainsboro, NJ 08536 USA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm) , Sterile; Integra LifeSciences Corporation, 311 Enterprise Drive, Plainsboro, NJ 08536 USA
Brand
Integra LifeSciences Corp
Lot Codes / Batch Numbers
Catalog Number 38101, Lot Number 105BA0121823
Products Sold
Catalog Number 38101, Lot Number 105BA0121823
Integra LifeSciences Corp is recalling Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm) , Sterile; Integra LifeSciences Corp due to Product labeled with an expiration date on May 2010, while the actual expiration date should be April 2010.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product labeled with an expiration date on May 2010, while the actual expiration date should be April 2010.
Recommended Action
Per FDA guidance
The firm issued a letter titled URGENT-RECALL NOTICE to Integra Sales Reps on July 2, 2008. Contact Integra at 609-799-3297 if you have questions.
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
AL, CA, IN, NY, TN
Page updated: Jan 10, 2026