Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI: (01)10827002311418(17)250401(30)1\F1(10)LB1520598 (01)10827002311418(17)250314(30)1\F1(10)LB1522022 (01)10827002311418(17)250320(30)1\F1(10)LB1522024 (01)10827002311418(17)250320(30)1\F1(10)LB1523113 (01)10827002311418(17)250401(30)1\F1(10)LB1524938 (01)10827002311418(17)250320(30)1\F1(10)LB1525251 (01)10827002311418(17)250408(30)1\F1(10)LB1525812 (01)10827002311418(17)250416(30)1\F1(10)LB1525827 (01)10827002311418(17)250416(30)1\F1(10)LB1525839 (01)10827002311418(17)250416(30)1\F1(10)LB1525923 (01)10827002311418(17)250410(30)1\F1(10)LB1525956 (01)10827002311418(17)250426(30)1\F1(10)LB1527864 (01)10827002311418(17)250424(30)1\F1(10)LB1529682 Lot Number: LB1520598 LB1522022 LB1522024 LB1523113 LB1524938 LB1525251 LB1525812 LB1525827 LB1525839 LB1525923 LB1525956 LB1527864 LB1529682
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Cook Biotech, Inc.
Reason for Recall:
Products expire prior to the expiration date printed on the product labeling
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603

Product Codes/Lot Numbers:

UDI: (01)10827002311418(17)250401(30)1\F1(10)LB1520598 (01)10827002311418(17)250314(30)1\F1(10)LB1522022 (01)10827002311418(17)250320(30)1\F1(10)LB1522024 (01)10827002311418(17)250320(30)1\F1(10)LB1523113 (01)10827002311418(17)250401(30)1\F1(10)LB1524938 (01)10827002311418(17)250320(30)1\F1(10)LB1525251 (01)10827002311418(17)250408(30)1\F1(10)LB1525812 (01)10827002311418(17)250416(30)1\F1(10)LB1525827 (01)10827002311418(17)250416(30)1\F1(10)LB1525839 (01)10827002311418(17)250416(30)1\F1(10)LB1525923 (01)10827002311418(17)250410(30)1\F1(10)LB1525956 (01)10827002311418(17)250426(30)1\F1(10)LB1527864 (01)10827002311418(17)250424(30)1\F1(10)LB1529682 Lot Number: LB1520598 LB1522022 LB1522024 LB1523113 LB1524938 LB1525251 LB1525812 LB1525827 LB1525839 LB1525923 LB1525956 LB1527864 LB1529682

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3261-2024

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