RegWardenFDA facility compliance records
Recall

Class II — OMM Imports, Inc. dba Zero Gravity

Recalling firmOmm Imports, Inc. d/b/a Zero Gravity
Registered facilityOMM IMPORTS, INC. D/B/A ZERO GRAVITY (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonThe firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information, reproductions and locations of the labels, and a warning statement in the user manual.
ProductRecreo Hair Growth Laser Comb
Quantity1620 units shipped to United States
DistributionWorldwide and Nationwide including DC and Puerto Rico
Initiated2022-09-01
Classified2023-03-14
Recall numberZ-1222-2023
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — OMM Imports, Inc. dba Zero Gravity (Z-1222-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91839/

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