{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "124437",
      "product_res_number": "Z-0730-2014",
      "event_date_initiated": "2013-11-04",
      "event_date_posted": "2014-01-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-10-08",
      "res_event_number": "66990",
      "product_code": "MBB",
      "k_numbers": [
        "K031673"
      ],
      "product_description": "Palacos R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl Methacrylate Monomer 0.5 g Gentamicin, Distributed by Zimmer Dover, OH 44522\r\n\r\nThe cement is indicated for use in the second stage of a two stage revision for total joint arthroplasty after the initial infection has been cleared.",
      "code_info": "Cat No. 00-1113-140-01; lot 75974340",
      "firm_fei_number": "1000220733",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "345 E Main St",
      "city": "Warsaw",
      "state": "IN",
      "postal_code": "46580-2746",
      "additional_info_contact": "800-613-6131",
      "reason_for_recall": "The patient label associated with the product may be incorrect in that the lot number on the patient label may be different than the lot number on the outer carton label.",
      "root_cause_description": "Other",
      "action": "Zimmer sent an Urgent Device Removal letter dated November 18, 2013, to all affected customers.  The letter identified the product, the problem, and the action to be taken by the customer.  Customers were instructed to review the notification, idetntify the product and remove from use.  If the affected product has been utilized, follow institutional protocol to determine if it is appropriate to place a copy of  the notification letter into patient records for the affected product.  Complete the attached Response Form and return it via fax to 800-871-7270.  Customers were instructed to return a copy of the completed response form along with their returned product to ensure proper credit.  Customers with questions were instructed to call 866-608-3941.\r\nFor questions regarding this recall call 800-613-6131.",
      "product_quantity": "1,534 units",
      "distribution_pattern": "Nationwide Distribution including AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, NC, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, VT, WA, WI, WV & WY.",
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        ],
        "device_name": "Bone Cement, Antibiotic",
        "medical_specialty_description": "Orthopedic",
        "regulation_number": "888.3027",
        "device_class": "2"
      }
    }
  ]
}