Home › Focus Health Group, Inc. › Zeni Medical
Zeni Medical
Focus Health Group, Inc. · Model 41048 · UDI-DI 00324357410047
1
510(k) clearances
4
Adverse events
9
Recalls
38
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
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.