{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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      "product_res_number": "Z-0384-05",
      "event_date_initiated": "2000-09-28",
      "event_date_posted": "2005-01-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-04-01",
      "res_event_number": "30656",
      "product_code": "MMP",
      "k_numbers": [
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      "code_info": "Lot Number A 7611",
      "firm_fei_number": "1625657",
      "recalling_firm": "Hydro Med Products, Inc",
      "address_1": "2930 Ladybird Ln",
      "city": "Dallas",
      "state": "TX",
      "postal_code": "75220-1417",
      "reason_for_recall": "Defective packaging, potential for breech in sterility.",
      "root_cause_description": "Other",
      "action": "The firm initiated the recall on 09/28/00 via letter.  The firm followed up with phone call contact to 100% of customers.",
      "product_quantity": "35 cases, 10 units per case",
      "distribution_pattern": "The product was distributed nationwide to distributors and hospitals in the following states IA, WV, OR, PA, CA, and TN",
      "openfda": {
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        "device_name": "Cover, Barrier, Protective",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4370",
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}