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Kit, Assay, Estrogen Receptor

FDA product code LPJ · Class 3 · Hematology

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

Recent recalls

DateFirmReason
2024-02-27Howmedica Osteonics Corp.The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

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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.