# Class II recall Z-0137-2027: Medtronic Sofamor Danek USA Inc

**Predicate Speed & CAPA Advisory Opportunity Score:** 68/100

| Field | Value |
|---|---|
| Record | Device recall |
| Recall number | Z-0137-2027 |
| Recalling firm | Medtronic Sofamor Danek USA Inc |
| Classification | Class II |
| Status | Ongoing |
| Voluntary / mandated | Voluntary: Firm initiated |
| Specialty | Other |
| Product | Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue  combined with an inert additive to yield a demineralized bone matrix (DBM)  allograft product having a particular physical form and/or handling property.  Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form  of DBM, while Grafton DBM Flex, Putty, Matrix, Crunch" and Orthoblend are  produced from a fiber form of DBM Crunch" also contains demineralized bone  chips/cubes, while Grafton DBM Orthoblend contains non-demineralized  cancellous bone chips in addition to DBM. Grafton DBM and Grafton Plus D |
| Reason | Medtronic identified through donor record review that the donor for Medtronic  batch A62881 did not meet all Medtronic donor eligibility requirements related to  the presence of microbial organisms.  While the batch passed finished product  sterility testing Medtronic is retrieving any unused product manufactured from the  donor tissue.    Donor bone tissue tested positive for Clostridium butyricum and while tissue did undergo gamma radiation, if implanted, there is a possibility of clostridium infection |
| Quantity | 18 |
| Distribution | US Nationwide distribution in the states of OK, VA, CO, AR, FL, TX, MD, DE, IL, MI, KS, AL, GA. |
| Recall initiated | 2026-08-12 |
| Reported | 2026-10-21 |
| Firm location | Memphis, TN, United States |

## Why this score
- Class II recall: usually triggers CAPA and quality-system remediation work.
- Recall is still ongoing.
- Posted 14 days ago.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0137-2027%22). Last refreshed: 2026-11-03T18:05:14.713Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.