{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Allentown",
      "address_1": "901 Marcon Boulevard",
      "reason_for_recall": "Firm became aware of the potential for breakage of the anti free flow clip catch, located on the inside of the pump door, when the IV set anti free flow clip is incorrectly inserted into the pump and the pump door forced closed.  If the clip catch is broken and the door opened, free flow protection is still ensured.  However, after the set is manually removed from the pump without the closure of t",
      "address_2": "",
      "product_quantity": "38,225 pumps",
      "code_info": "Pump Model Numbers: 8713050U, 8713050U-99, 8713050US, 8713060U, and 8713060U-99  --  various serial numbers.",
      "center_classification_date": "20120716",
      "distribution_pattern": "Nationwide Distribution-including Puerto Rico and the states of AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, TN, TX, VT, VA, WA, WV, and WI.",
      "state": "PA",
      "product_description": "Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005, 686F030007, 686G030002, and 686G030102.    Intended for use with adults, pediatrics and neonates and is intended to provide infusions of parenteral fluids/medications, blood and blood products indicated for infusion through FDA approved routes of administration.",
      "report_date": "20120725",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "B. Braun Medical, Inc.",
      "recall_number": "Z-1992-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62115",
      "termination_date": "20141103",
      "more_code_info": "",
      "recall_initiation_date": "20120323",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}