Home › Device types › OBK
Port, Protector/Cushion
FDA product code OBK · Class 2 · General Hospital
0
Registered devices
0
Adverse events
1
Recalls
1
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-09-10 | Baxter Healthcare Corp. | The firm is recalling lots 10043 and 10044 due to loose particulate matter found in the packaging. Particulate matter entering the fluid path from the Luer lock |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.