{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Natick",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94124",
      "recalling_firm": "InfuTronix LLC",
      "address_1": "177 Pine St",
      "address_2": "N/A",
      "postal_code": "01760-1331",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic US distribution nationwide. No international distribution.",
      "recall_number": "Z-1285-2024",
      "product_description": "Nimbus Administration Set;  Nimbus Flex;  Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System);   Catalog Number IT1025.  Ambulatory Infusion Pump and components",
      "product_quantity": "52,328 total",
      "reason_for_recall": "InfuTronix is removing the Nimbus Infusion Pump Systems from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing. The device will not be available or supported after June 20, 2024.",
      "recall_initiation_date": "20240221",
      "center_classification_date": "20240328",
      "report_date": "20240403",
      "code_info": "UDI-DI 00817170020000 Lots  A100-150205200 A100-150415015 A100-150430270 A100-150611300 A100-150716620 A100D-1705191000 AZ060-171201564 AZ060-1801021020 AZ060-180609264 AZ060-180626552 AZ060-190104792 AZ060-1902151200 A100F-160707073 A100F-160908250 A100F-161114700  All units recalled",
      "more_code_info": ""
    }
  ]
}