{
  "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": "Lake Forest",
      "address_1": "600 N Field Dr",
      "reason_for_recall": "A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.",
      "address_2": "",
      "product_quantity": "180 units",
      "code_info": "List number: 11005;  Serial Numbers:   16792201  16792202  16792205  16792206  16792208  16792209  16792210  16792211  16792213  16792216  16792217  16792219  16792220  16792222  16792223  16792224  16792225  16792226  16792227  16792228  16792230  16792232  16792233  16792234  16792235  16792236  16792238  16792239  16792240  16792241  16792242  16792244  16792245  16792246  16792248  16792249  16792250  16792251  16792252  16792253  16792254  16792255  16792256  16792257  16792258  16792259  16792260  16792261  16792263  16792264  16792265  16792266  16792268  16792269  16792271  16792272  16792273  18807402  18807405  18807406  18807407  18807408  18807409  18807410  18807413  18807414  18807417  18807418  18807420  18807421  18807423  18807427  18807428  18807429  18807430  18807431  18807432  18807433  18807434  18807439  18807443  18807444  18807446  18807449  18807452  18807453  18807455  18807456  18807459  18807463  18807466  18807472  18807474  18807478  18807484  18807485  18807486  18807490  18807491  18807494  18807496  18807499  18807500  18807501  18807506  18807509  18807510  18807511  18807513  18807514  18807518  18807523  18807524  18807529  18807535  18807536  18807539  18807540  18807541  18807542  18807543  18807545  18807546  18807556  18807557  18807568  18807574  18807575  18807576  18807578  18807581  18807584  18807585  18807586  18807588  18807589  18807590  18807591  18807592  18807596  18807597  18807598  18807599  18807600  18807601  18807602  18807604  18807605  18807607  18807608  18807609  18807610  18807611  18807612  18807613  18807614  18807617  18807618  18807619  18807620  18807623  18807625  18807626  18807627  18807628  18807630  18807631  18807632  18807633  18807634  18807636  18807637  18807639  18807640  18807695  18807696  18807697  18807698  18807699  18807700",
      "center_classification_date": "20170710",
      "distribution_pattern": "Nationwide, Worldwide",
      "state": "IL",
      "product_description": "The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ICU",
      "recall_number": "Z-2675-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64542",
      "termination_date": "20180531",
      "more_code_info": "",
      "recall_initiation_date": "20130201",
      "postal_code": "60045-4835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}