Home › Device types › LLD
Port & Catheter, Implanted, Subcutaneous, Intraperitoneal
FDA product code LLD · Class 2 · General Hospital
260
Registered devices
16
Adverse events
6
Recalls
4
510(k) clearances
Devices with this code
M SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationR SERIES — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationR SERIES — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical CorporationM SERIES BIPHASIC — Zoll Medical Corporation
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
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