{
  "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": [
    {
      "status": "Terminated",
      "city": "Richmond",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88561",
      "recalling_firm": "Cypress Medical Products LLC",
      "address_1": "9954 Mayland Dr",
      "address_2": "N/A",
      "postal_code": "23233-1464",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "VA",
      "recall_number": "Z-2473-2021",
      "product_description": "McKesson Lap Sponge, X-Ray Detectable \t12\"x 12\", 5/pack, Sterile McKesson Part #\t16-2112121",
      "product_quantity": "1 case (40 packs/cs)",
      "reason_for_recall": "Manufacturer issued a recall due to an EO indicator color. The indicator should change from red to blue signifying sterilization. However, on one case of product, the indicators did not change",
      "recall_initiation_date": "20210811",
      "center_classification_date": "20210914",
      "termination_date": "20230707",
      "report_date": "20210922",
      "code_info": "Lot number: CJJ12-07",
      "more_code_info": ""
    }
  ]
}