Recall Z-0834-2025 ยท GXQ Dura Substitute
Cook Biotech, Inc.
Cook Medical Biodesign Dural Graft, REF C-DUR-7X10, REF G31091, Sterile
| Date | Jan 10, 2025 (initiated Nov 22, 2024) |
| Status | Open, Classified |
| Reason | Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products. |
| Root cause | Under Investigation by firm |
| Action | The recalling firm issued two different emails on 11/22/2024, one informing the direct account that the devices either had an incorrect IFU revision (Biodesign Otologic Butterfly Graft, ENT-OTO-BFLY-0.4-0.6) or had an incorrect expiration date (Biodesign Hiatal Hernia Graft, C-PHR, and Biodesign Dural Graft, C-DUR); and the other informing a different direct account that the product had an incorrect IFU revision for two lots (for Biodesign Otologic Butterfly Graft, ENT-OTO-BFLY-0.4-0.6). The direct accounts informed the recalling firm, and the recalling firm issued "URGENT: MEDICAL DEVICE REC |
| Quantity | 10 devices |
| Distribution | US (domestic) Distribution to states of IN and MI; and OUS (foreign) to Canada and South Korea. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K160869 | Biodesign Tissue Graft, Biodesign Dural Graft, Biodesign Peyronie's Repair Graft Cook Biotech Incorporated, Apr 29, 2016 |