{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86462",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "150 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  AE, AT, AU, BE, BM, BR, CA, CH, CL, CN, CO, CY,  CZ, DE, DK, DO, EC, EE, ES, FI, FR, GB, GE, GR, HK,  HU, IE, IL, IN, IT, JP,KR, LV,MY, NL, NO, PA,PE, PL,  PR, PT, RU, SE, SG, SI, TH, TR, TW, UA,  & ZA",
      "recall_number": "Z-0153-2021",
      "product_description": "OSTEORAPTOR 2.9 W. 2 UB WHITE / BLACK  -Absorbable Suture anchor  Product Number: 72201996",
      "product_quantity": "N/A",
      "reason_for_recall": "Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch",
      "recall_initiation_date": "20200909",
      "center_classification_date": "20201021",
      "report_date": "20201028",
      "code_info": "Batch Numbers:  2012912  2017844  2019840  2021496  2024714  2033500  2049663  2052725  2055727"
    }
  ]
}