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Containment System, Laparoscopic Power Morcellation, With Instrument Port

FDA product code PMU · Class 2 · Obstetrics/Gynecology

5
Registered devices
12
Adverse events
1
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-09-21Olympus Corporation of the AmericasDue to manufacturing error, the Pneumoliner Bag Distal Tab that exits the Introducer shaft is in the wrong orientation. This results in the user deploying the b

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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.