{
  "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": [
    {
      "status": "Terminated",
      "city": "Orange",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63557",
      "recalling_firm": "Kerr Corporation",
      "address_1": "1717 W Collins Ave",
      "address_2": "N/A",
      "postal_code": "92867-5422",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Canada, Europe, Australia and ROW consignees  .",
      "recall_number": "Z-0401-2013",
      "product_description": "BioPlant, a dental bone grafting material. BioPlant  has been assigned the product code LYC (Bone Grafting Material, Synthetic) by the  FDA and is classified as a Class II Medical Device.   BioPlant is a Class II Medical Device. The Device Listing Number is 0007254.    BioPlant is a synthetic, multipurpose bone-grafting material intended to be used in dental applications to maintain and restore the bony alveolar ridge in post-extraction tooth-root sockets or after oral surgery, ridge preservation, ridge augmentation, augmentations in the maxillary sinus, repair of periodontal defects and bone voids associated with dental implant placement.",
      "product_quantity": "22,410 units",
      "reason_for_recall": "The firm initiated the recall becaue disturbing the BioPlant product soon after it is placed may halt or delay the ossification process.",
      "recall_initiation_date": "20121025",
      "center_classification_date": "20121120",
      "termination_date": "20130923",
      "report_date": "20121128",
      "code_info": "The BioPlant part numbers and lot numbers affected by this recall are as follows:    Product Description                     Part Numbers  Lot Numbers     BioPlant Curved Syringe, 0.125g  216110  All Production     BioPlant Curved Syringe, 0.25g  216112     BioPlant Curved Svrinoe, 0.50<1  216114  Lots Within Shelf-Life    BioPlant Curved Svrinoe, 0.250  216132       20k    BioPlant Intro Pack   216112S"
    }
  ]
}