Genzyme Corporation Seprafilm Adhesion Barrier (chemically modified sodium hyaluronate/carboxymethylcellulose absorbable adhesion barrier) Product Number: 4301-02 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Seprafilm Adhesion Barrier (chemically modified sodium hyaluronate/carboxymethylcellulose absorbable adhesion barrier) Product Number: 4301-02
Brand
Genzyme Corporation
Lot Codes / Batch Numbers
Lot Numbers: 07NP135 Exp Date: April 2010, 07NP177 Exp Date: May 2010, 07NP199 Exp Date: June 2010, 07NP216 Exp. Date: July 2010, 07NP311 Exp. Date: May 2010
Products Sold
Lot Numbers: 07NP135 Exp Date: April 2010; 07NP177 Exp Date: May 2010; 07NP199 Exp Date: June 2010; 07NP216 Exp. Date: July 2010; 07NP311 Exp. Date: May 2010
Genzyme Corporation is recalling Seprafilm Adhesion Barrier (chemically modified sodium hyaluronate/carboxymethylcellulose absorbable due to Sterility may be compromised. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility may be compromised
Recommended Action
Per FDA guidance
Genzyme notified Distributors and hospitals by letter dated 4/10/08, requesting ceasing distribution and return recalled product.
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 noticePage updated: Jan 10, 2026