Home › Howmedica Osteonics Corp. › Dall-Miles
Dall-Miles
Howmedica Osteonics Corp. · Model 3704-2-091 · UDI-DI 07613154490301
2
510(k) clearances
31
Adverse events (1 deaths)
4
Recalls
7
Facilities
Description
Trochanteric grip plate
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-06-21 | Ossur Americas | Halo system products labeled MR conditional will undergo confirmatory safety testing to confirm MR conditional parameters. In addition, the second line description on the titanium |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.