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Recall Observatory FDA recall evidence

Device product

GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02

Z-0233-2023

October 14, 2022

Class II

Product summary

Firm
Sonendo Inc
Event
Event 91045
Status
Ongoing
Classification
Class II
Quantity
15 instruments
Official record key
device-enforcement:Z-0233-2023

Official wording

Reason: Procedure Instruments with erroneous unit carton labels.

Code information: GentleWave System Anterior/Premolar Procedure Instrument (GW-APM-PI02) UDI-DI Code: 00858395006318 Lot Number: W2022080941R

Distribution pattern: Worldwide - U.S. Nationwide distribution in the state of OH and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Procedure Instruments with erroneous unit carton labels.