{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "218003",
      "product_res_number": "Z-1165-2026",
      "event_date_initiated": "2025-12-29",
      "event_date_posted": "2026-01-23",
      "recall_status": "Open, Classified",
      "res_event_number": "98242",
      "product_code": "NOX",
      "pma_numbers": [
        "P240001"
      ],
      "product_description": "PearMatrix P-15 Peptide Enhanced Bone Graft\nBone Graft, 1.0cc\nREF: 730-010",
      "code_info": "Lot: 7014819/UDI: (01)00850001680196",
      "firm_fei_number": "3007155473",
      "recalling_firm": "Cerapedics, Inc.",
      "address_1": "11025 Dover St Unit 1600 11025 Dover St",
      "address_2": "Unit 1600",
      "city": "Westminster",
      "state": "CO",
      "postal_code": "80021-5574",
      "additional_info_contact": "Rebecca Helpert\n510-333-1697",
      "reason_for_recall": "Incorrect expiration date",
      "root_cause_description": "Labeling Change Control",
      "action": "On December 29, 2025, Cerapedics issues a \"Urgent: Medical Device Recall\" notification to affected consignees via Email. Cerapedics asked consignees to take the following actions:\n\n1.\tPlease immediately examine your inventory and return any remaining units of PearlMatrix 1.0cc, lot 7014819. \n\"\tRMA will be issued for this return and a shipping label.\n2.\tPlease acknowledge receipt of this letter by responding to this email or call toll-free at 1-866-360-5612.   \n3.\tIf you have further distributed this product, please identify your customers, and notify them at once of this product recall.  You may provide a copy of this recall notification letter to your customer.",
      "product_quantity": "237 units",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CO, CT, FL, GA, ID, IL, KS, LA, MI, MN, MO, MT, NE, NJ, NV,  NY, OH,OR, PA, TN, TX, WA, WY.",
      "openfda": {
        "pma_number": [
          "P140019",
          "P240001",
          "P100006"
        ],
        "device_name": "Filler, Bone Void, Synthetic Peptide",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "registration_number": [
          "3003897776",
          "3010667733",
          "2530154",
          "3007155473",
          "2245304",
          "1043534"
        ],
        "fei_number": [
          "3003897776",
          "3010667733",
          "3007155473",
          "2245304",
          "1000307073",
          "1043534"
        ]
      }
    }
  ]
}