{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cleveland",
      "address_1": "913 N Davis Ave",
      "reason_for_recall": "Subpotent",
      "address_2": "",
      "product_quantity": "7,711 syringes",
      "code_info": "Service Code 2K2466 and 2K2470    183320004S, 183330008S, 183340002S, 183340003S, 183300004S, 183310007S, 183370041S, 183310043S, 183370042S, 183320003S, 183380007S, 183250013S, 183250014S, 183320005S, 183330009S, 183370007S, 183390044S, 183400006S, 183410003S.",
      "center_classification_date": "20190114",
      "distribution_pattern": "Product was distributed throughout the United States.",
      "state": "MS",
      "product_description": "0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) a.) 1 mL in 3 mL BD Syringe, 10 per carton, b.) 0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) 5 mL in 5 mL BD Syringe, 10 per carton Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478.",
      "report_date": "20190116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "PharMEDium Services, LLC.",
      "recall_number": "D-0374-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81895",
      "termination_date": "20200507",
      "more_code_info": "",
      "recall_initiation_date": "20190102",
      "postal_code": "38732-2106",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}