{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-17",
    "results": {
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      "product_res_number": "Z-1222-2023",
      "event_date_initiated": "2022-09-01",
      "event_date_posted": "2023-03-14",
      "recall_status": "Open, Classified",
      "res_event_number": "91839",
      "product_code": "OAP",
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      "product_description": "Recreo Hair Growth Laser Comb",
      "code_info": "Class 3R Zero Gravity Recreo Hair Growth Laser Comb",
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      "recalling_firm": "OMM Imports, Inc. dba Zero Gravity",
      "address_1": "940 Lincoln Rd Ste 307 940 Lincoln Rd",
      "address_2": "Ste 307",
      "city": "Miami Beach",
      "state": "FL",
      "postal_code": "33139-2619",
      "additional_info_contact": "Lisa Capote \n786-871-5683",
      "reason_for_recall": "The 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.",
      "root_cause_description": "Error in labeling",
      "action": "Letters were sent to all retailers/distributors and any direct purchasers advising of the affected device nonconformance.   The letter informed customers that an updated user manual and the appropriate labels will be provided to correct the error, without charge.",
      "product_quantity": "1620 units shipped to United States",
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