Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France InterGard Knitted Collagen Coated Vascular prostheses, Catalog number: IGK1206. InterVascular SAS, France. Indicated for surgical repair, bypass or replacement of arteries in the treatment of aneurysmal and occlusive disease of the abdominal aorta, visceral arteries, and peripheral arteries. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
InterGard Knitted Collagen Coated Vascular prostheses, Catalog number: IGK1206. InterVascular SAS, France. Indicated for surgical repair, bypass or replacement of arteries in the treatment of aneurysmal and occlusive disease of the abdominal aorta, visceral arteries, and peripheral arteries.
Brand
Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France
Lot Codes / Batch Numbers
Serial Number: 40246657, Lot number: 09M03.
Products Sold
Serial Number: 40246657, Lot number: 09M03.
Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France is recalling InterGard Knitted Collagen Coated Vascular prostheses, Catalog number: IGK1206. InterVascular SAS, due to Packaging was mislabeled.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Packaging was mislabeled.
Recommended Action
Per FDA guidance
InterVascular SAS issued a "Recall Notification - Product Recall RC 020" notification dated January 29, 2009 to the sole consignee. The consignee had previously been notified by phone and all affected product had been segregated. For further information, contact InterVascular SAS at +33 442 08 77 84.
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