{
  "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-0172-2021",
      "product_description": "HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- Absorbable Suture anchor  Product Number: 72203708",
      "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:  2014002  2016196  2017814  2020051  2021388  2023272  2024724  2026266  2024759  2025289  2027469  2030955  2031023  2033400  2035501  2036291  2038328  2039263  2048404  2049924  2051020  2053921  2056432  2057402"
    }
  ]
}