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ASEPT
B BRAUN INTERVENTIONAL SYSTEMS, INC · Model 622284 · UDI-DI 04046964317330
PNG
Prescription
2
510(k) clearances
178
Adverse events (2 deaths)
13
Recalls
28
Facilities
Description
ASEPT PERITONEAL DRAINAGE SYSTEM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
| 2023-04-22 | Merit Medical Systems, Inc. | There is a potential that valve assemblies will not open. preventing fluid from draining. |
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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.
