{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allendale",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73179",
      "recalling_firm": "Stryker Spine",
      "address_1": "2 Pearl Ct",
      "address_2": "N/A",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0852-2016",
      "product_description": "AccuLIF PL Tubing Set and AccuLIF TL Tubing Set    AccuLIF is an interbody device system that uses hydraulic pressure to expand the implant in-situ. The purpose of the AccuLIF PL Tubing Set  (cat#900301) and AccuLIF TL Tubing Set (cat#905103) is to deliver pressurized saline from a syringe to the AccuLIF implant for in-situ expansion. The Tubing Set attaches to the AccuLIF Insertion handle at two district locations: the \"junction block\" and the \"manifold.\" The PL and TL Tubing Sets are Class 2 instruments not intended to sustain or support life.",
      "product_quantity": "413 units",
      "reason_for_recall": "There were two potential interference conditions identified with the way the tubing set attaches to the inserter.",
      "recall_initiation_date": "20151216",
      "center_classification_date": "20160223",
      "termination_date": "20160801",
      "report_date": "20160302",
      "code_info": "Catalog number 900301, Lot #01131543, 01261508, 10151404, 10271408, 12161403, 12161404, 09021404, 01261509, 10271407, 01261507, 10071415, 05011403, 06241407, 08071402, 10091305, 03041403, 01271412, 07281401, and 11061303.  Catalog number  905103, 01131542, 11241408, 12161405, 12161406, 0211501, 01211502, 11241406, 02031403, 06241408, 07161407, 09101402, 09281401, 10251303, 05301402, 11241407, and 12101305.",
      "more_code_info": ""
    }
  ]
}