{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bolton",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90849",
      "recalling_firm": "Medicina Uk Ltd",
      "address_1": "Unit 2",
      "address_2": "Rivington View Business Park",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0107-2023",
      "product_description": "Medicina ENFit 1ml Reusable Low Dose Enteral Syringe    Code: LHE01LD",
      "product_quantity": "9 boxes (900 syringes)",
      "reason_for_recall": "Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification",
      "recall_initiation_date": "20220704",
      "center_classification_date": "20221020",
      "report_date": "20221026",
      "code_info": "UDI-DI: (01)05060278508146  Batch number: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018",
      "more_code_info": ""
    }
  ]
}