Home › Device types › FIK
System, Dialysate Delivery, Recirculating
FDA product code FIK · Class 2 · Gastroenterology, Urology
0
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-04-03 | Baxter Healthcare Corp. | Additional warning in the AMIA APD System labeling for patients vulnerable to unintended Increased Intraperitoneal Volume (IIPV), also known as overfill. The pa |
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