{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "104145",
      "product_res_number": "Z-0081-2012",
      "event_date_initiated": "2011-07-28",
      "event_date_posted": "2011-10-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-12-19",
      "res_event_number": "59981",
      "product_code": "MEB",
      "k_numbers": [
        "K081905"
      ],
      "product_description": "Medpro AccuFlo Elastomeric Infusion Device, Model #CT-0020-270C, packaged 12/box.   The box label shows the product is Manufactured By: Medpro International (Thailand) Ltd. for Medpro Corporation Pte. Ltd., Singapore.\n\nThe devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications.",
      "code_info": "Lot #100924, Exp. 2015-08, Item CT-0020-270C",
      "firm_fei_number": "3000236238",
      "recalling_firm": "Progressive Medical Inc",
      "address_1": "11085 Gravois Industrial Ct",
      "city": "Saint Louis",
      "state": "MO",
      "postal_code": "63128-2012",
      "additional_info_contact": "Mark M. Martin\n314-961-5786",
      "reason_for_recall": "The product may have a higher flow rate than specified resulting in over administration of drug solutions to the patients.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "The firm, Progressive Medical, sent an \"URGENT: MEDICAL DEVICE RECALL\" letter dated July 28, 2011 via email and regular mail to its customers.  The letter describes the product, problem and actions to be taken. The customers were instructed to discontinue their use; remove the products from inventory  and quarantine them; inform their customers to return unused products to Progressive; return the product, and complete and return the RECALL RETURN RESPONSE FORM via fax to 314-961-5786. \n\nProgressive customer service will contact the customers to coordinate the return of the goods in question.\n\nShould you have any questions, please call 800-969-6331 or email to dsullivan@progressivemedinc.com.",
      "product_quantity": "180 units",
      "distribution_pattern": "Nationwide distribution: USA including states of: FL, KY, PA, VA and WY.",
      "openfda": {
        "k_number": [
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        ],
        "registration_number": [
          "3003898360",
          "3013764800",
          "",
          "2029275",
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          "3024702421",
          "2025695",
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          "9680787"
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        "fei_number": [
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          "3024702421",
          "1000138054",
          "3002826093",
          "2025695",
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          "1416980",
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          "1000306431",
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          "3002806575",
          "3005747797",
          "3004365956",
          "3002907620",
          "3010055973",
          "3000206435"
        ],
        "device_name": "Pump, Infusion, Elastomeric",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
      }
    }
  ]
}