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FDA product code INQ · Class 1 · Physical Medicine

1,046
Registered devices
47
Adverse events
2
Recalls
102
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-06-29ARJOHUNTLEIGH POLSKA Sp. z.o.o.ArjoHuntleigh has concluded that a device tipping hazard may occur on the current Sara Combilizer lifting mechanism, providing a potential for risk to the patie
2009-01-26Phillips Nuclear MedicineA problem has been identified with some upper patient pallets on Precedence SPECT/CT System, which may reduce its load bearing capacity and may result in its cr

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