{
  "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": "156766",
      "product_res_number": "Z-0196-2018",
      "event_date_initiated": "2017-05-22",
      "event_date_created": "2017-12-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-02-26",
      "res_event_number": "77609",
      "product_code": "JSO",
      "product_description": "TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261\nTrypticase Soy Agar with 5% or 10% Sheep Blood is used for cultivating fastidious microorganisms and for the visualization of hemolytic reactions produced by many bacterial species.",
      "code_info": "Lot Number: 7032978 - Exp Date May 24, 2017                         7048902 - Exp Date June 9, 2017",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152-9212",
      "additional_info_contact": "410-316-4000",
      "reason_for_recall": "Listeria monocytogenes contamination of non-sterile plated media",
      "root_cause_description": "Material/Component Contamination",
      "action": "BD Life Sciences initiated communication with distributors by issuing Urgent Product Recall and Customer Response Form notices via UPS mailing on May 22, 2017.  General customers were issued Urgent Product Recall and Customer Response Form letters via UPS mailing on May 25, 2017.  \n- General customers were advised to visually inspect all non-sterile prepared media prior to use to assure that there is no surface and/or subsurface contamination.  If the customer observes a plate without evidence of microbial contamination that grows Listeria, please consult the clinician to make sure this result is consistent with the patient's clinical presentation.  \n- Distributors were advised  to discontinue distribution of the lots and to discard any remaining inventory.  Customers are advised to complete and return the enclosed response form to: Attention: Regulatory Compliance, Fax: 410-316-4258 or email to BDRC2@bd.com   \n**Note to Distributors:  Please provide BD Regulatory Compliance an Excel file or a list with name, address and telephone number of end-users who were shipped this product from their distribution branches so they can be notified.  Mail or fax to: BD Regulatory Compliance 7 Loveton Circle Mail Stop 640, Sparks, MD 21152 Fax: 410-316-4258; Email: BDRC2@bd.com.\nCustomers with questions please contact BD Support at 1-800-638-8663.  For customers outside of the U.S., contact your local BD representative or distributor.\nFor questions regarding this recall call 410-316-4000.",
      "product_quantity": "250, 300 plates",
      "distribution_pattern": "Worldwide Distribution - US including AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, FA, HI, IA, IS, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT & WA; International - Canada, Guam and Japan",
      "openfda": {
        "k_number": [
          "K070361",
          "K951754",
          "K102922",
          "K092407",
          "K770441",
          "K162620",
          "K190553",
          "K881568",
          "K122187",
          "K160512",
          "K081212",
          "K903425",
          "K945569",
          "K972359",
          "K881567",
          "K092819",
          "K091025",
          "K103684",
          "K952595",
          "K962744",
          "K073027",
          "K932882",
          "K892928",
          "K941443",
          "K100589",
          "K151688",
          "K894848",
          "K091024",
          "K932879",
          "K181092",
          "K171061",
          "K092767",
          "K964560",
          "K162076",
          "K944554",
          "K042812",
          "K923892",
          "K894216",
          "K941444",
          "K811513"
        ],
        "registration_number": [
          "1111096",
          "1924669",
          "1119779",
          "9615755",
          "3035708936",
          "3013394941",
          "8010096",
          "8023060",
          "3009307598",
          "2022807",
          "3009547954"
        ],
        "fei_number": [
          "1111096",
          "1924669",
          "3007808629",
          "1119779",
          "3006224287",
          "3003992026",
          "3035708936",
          "3013394941",
          "3009307598",
          "2022807",
          "3009547954"
        ],
        "device_name": "Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.1700",
        "device_class": "2"
      }
    }
  ]
}