{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
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  "results": [
    {
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      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        ],
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        ],
        "route": [
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        "rxcui": [
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          "43598-666-25"
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        "upc": [
          "0343598666259",
          "0343598666112"
        ],
        "unii": [
          "I9L0DDD30I"
        ]
      },
      "product_type": "Drugs",
      "event_id": "97690",
      "recalling_firm": "Dr. Reddy's Laboratories, Inc.",
      "address_1": "600 College Rd E Ste 4000",
      "address_2": "",
      "postal_code": "08540-6636",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the USA.",
      "recall_number": "D-0008-2026",
      "product_description": "Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials, For Intravenous or Intramuscular use, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540.  NDC: 43598-666-25",
      "product_quantity": "571 vials",
      "reason_for_recall": "Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.",
      "recall_initiation_date": "20250926",
      "center_classification_date": "20251007",
      "report_date": "20251015",
      "code_info": "Lot # K250048",
      "more_code_info": ""
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}