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Antiserum, Digoxin

FDA product code DKA · Class 2 · Clinical Toxicology

0
Registered devices
0
Adverse events
1
Recalls
3
510(k) clearances

Recent recalls

DateFirmReason
2003-11-07Interpore Cross International IncStep drills from Lot 25947 may have been mis-etched.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.