Medtronic — Class II medical device recall Z-0698-2024
Ongoing recall by Medtronic Navigation, Inc., reported 2024-01-17, distributed nationwide. Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit in
| Recall number | Z-0698-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Navigation, Inc., Lafayette, CO, United States |
| Recall initiated | 2023-11-28 |
| Classified | 2024-01-10 |
| Reported by FDA | 2024-01-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CN, DE, DK, ES, FI, FR, GB, HK, HU, IE, IL, IT, JP, LU, NL, NZ, OM, PT |
| Quantity | 4,235 units |
| UPC / GTIN / UDI-DI | 00613994247872 |
| Serial numbers | 2023010549, 2023010551, 2023010840, 2023041134, 2023051137, 2023051138, 2023051139, 2023060368, 2023060369 |
| Model numbers | 100MM, 9733235 |
Product
Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
Reason for recall
Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0698-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.