{
  "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-0147-2021",
      "product_description": "RAPTORMITE 3.7MM AB W/ NEEDLES AND TWO-Absorbable Suture anchor  Product Number: 72201805",
      "product_quantity": "263,874 (total)",
      "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:  2025354  2031116  2040066  2040702  2042557  2049638  2053749  2055239"
    }
  ]
}