{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "55355",
      "product_res_number": "Z-0014-2008",
      "event_date_initiated": "2007-04-23",
      "event_date_posted": "2007-10-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-06-07",
      "res_event_number": "39382",
      "product_code": "JSO",
      "product_description": "Brain Heart Infusion Agar labeled  BHIA + Vancomycin 6 MCG/ML  For Screening for Vancomycin Resistant Enterococci  PML microbiologicals  Wilsonville, Oregon 97070 USA\n\nCatalog #P1174",
      "code_info": "Lot numbers 229957-1 and 229958-1",
      "firm_fei_number": "3017344",
      "recalling_firm": "Pml Microbiologicals Inc.",
      "address_1": "27120 Sw 95th Ave",
      "address_2": "P.o. Box 570",
      "city": "Wilsonville",
      "state": "OR",
      "postal_code": "97070",
      "additional_info_contact": "503-570-2500",
      "reason_for_recall": "Plates manufactured without vancomycin.  Possibility for false resistant results.",
      "root_cause_description": "Other",
      "action": "On 4/23/07 the firm began contacting customers via fax and telephone.",
      "product_quantity": "640 total plates, 320 per lot (lot 229957-1 was dist only in Canada; lot 229958-1 was dist in the US and Canada)",
      "distribution_pattern": "lot #229957-1:  120 plates were distributed to 9 Canadian consignees; 200 plates were shipped, quarantined, and destroyed at the Canadian distribution center.\n\nlot #229958-1:  110 plates were distributed to 9 US consignees; 210 plates were shipped, quarantined, and destroyed at the Canadian distribution center.",
      "openfda": {
        "k_number": [
          "K892928",
          "K941443",
          "K091025",
          "K092407",
          "K092819",
          "K151688",
          "K042812",
          "K881568",
          "K932882",
          "K894848",
          "K932879",
          "K181092",
          "K894216",
          "K944554",
          "K162076",
          "K070361",
          "K092767",
          "K160512",
          "K945569",
          "K073027",
          "K962744",
          "K190553",
          "K952595",
          "K811513",
          "K903425",
          "K923892",
          "K091024",
          "K964560",
          "K972359",
          "K941444",
          "K770441",
          "K951754",
          "K171061",
          "K100589",
          "K081212",
          "K122187",
          "K162620",
          "K881567",
          "K103684",
          "K102922"
        ],
        "registration_number": [
          "3009307598",
          "8023060",
          "2022807",
          "3035708936",
          "1924669",
          "8010096",
          "9615755",
          "1119779",
          "3009547954",
          "3013394941",
          "1111096"
        ],
        "fei_number": [
          "3009307598",
          "2022807",
          "3007808629",
          "3003992026",
          "3035708936",
          "1924669",
          "1119779",
          "3006224287",
          "3009547954",
          "3013394941",
          "1111096"
        ],
        "device_name": "Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.1700",
        "device_class": "2"
      }
    }
  ]
}