{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Suffern",
      "address_1": "25 Old Mill Rd",
      "reason_for_recall": "Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test during stability testing.",
      "address_2": "",
      "product_quantity": "19,658 packs",
      "code_info": "Lot #: F8011, Exp May 2015",
      "center_classification_date": "20150615",
      "distribution_pattern": "NJ via 1 distributor",
      "state": "NY",
      "product_description": "Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule,  12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx only, Manufactured for: Merck Sharp & Dohme Corp., a subsidiary of MERCK & CO., INC. Whitehouse Station, NJ 08889.  Manufactured by: Novartis Pharma AG Basle,Via Serafino Balestra 31 Locarno, Switzerland.",
      "report_date": "20150624",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Novartis Pharmaceuticals Corp.",
      "recall_number": "D-1137-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "71310",
      "termination_date": "20160518",
      "more_code_info": "",
      "recall_initiation_date": "20150522",
      "postal_code": "10901-4106",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}