Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic… — Class II medical device recall Z-0908-2014
Terminated recall by Medtronic Cardiovascular Surgery-the Heart Valve Division, reported 2014-02-12, distributed nationwide. Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305 used with the Mosaic Porcin
| Recall number | Z-0908-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Cardiovascular Surgery-the Heart Valve Division, Santa Ana, CA, United States |
| Recall initiated | 2014-01-09 |
| Classified | 2014-02-04 |
| Reported by FDA | 2014-02-12 |
| Terminated | 2014-05-30 |
| Distributed | Nationwide (US) |
| Quantity | 8,276 units |
| Model numbers | 7305, 7305C, 7305OD, 7305UX |
Product
Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
Reason for recall
Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305 used with the Mosaic Porcine Aortic Bioprosthesis, Model Number 305, because of higher-than-expected transvalvular gradients occurring post implant.
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-0908-2014. 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.