{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78762",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY, and Puerto Rico; and to countries of: Austria, Australia, Bahamas, Brazil, Canada, China, Dominican Republic, England, France, Germany, Israel, Japan, South Korea, Lebanon, Malaysia, Mexico, Netherlands, Panama, Singapore, Spain, Switzerland, and Thailand.",
      "recall_number": "Z-0721-2018",
      "product_description": "Zimmer Segmental System, ZSS Distal Femur.  Sizes as follows:    a. Size B-LT (Item No. 00585001201);    b. Size B-RT (Item No. 00585001202);    c. Size C-LT (Item No. 00585001301);    d. Size C-RT (Item No. 00585001302)    Components of the system are intended to replace the proximal femur, mid-shaft femur, distal femur, proximal tibia, and/or total knee in cases that require extensive resection and restoration.",
      "product_quantity": "3,350 units total",
      "reason_for_recall": "The products being recalled exceeded the weight previously tested leading to a possibility of damage to the package and/or a compromised sterile barrier.",
      "recall_initiation_date": "20170801",
      "center_classification_date": "20180226",
      "termination_date": "20200318",
      "report_date": "20180307",
      "code_info": "a. Item No. 00585001201 (Lot Expiration Date Before 07/31/2026);    b. Item No. 00585001202 (Lot Expiration Date Before 07/31/2026);    c. Item No. 00585001301 (Lot Expiration Date Before 08/31/2026);    d. Item No. 00585001302 (Lot Expiration Date Before 07/31/2026)"
    }
  ]
}