{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "El Dorado Hills",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64810",
      "recalling_firm": "Synvasive Technology Inc",
      "address_1": "4925 Robert J Mathews Pkwy",
      "address_2": "N/A",
      "postal_code": "95762-5701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and countries of: Austria, Australia, Belgium, Czech Republic, Denmark, Finland, France, Germany, Italy, Japan, Netherlands, Norway, Panama, Spain, Sweden, Switzerland, Tunisia, United Kingdom and Yemen.",
      "recall_number": "Z-1115-2013",
      "product_description": "Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under Synvasive Technology, Inc. El Dorado Hills, CA     Reciprocating saw blade: A sterile surgical saw blade used to resect damaged cartilage and/or bond in an orthopaedic reconstructive procedure such as a total knee replacement.",
      "product_quantity": "3442 units per the part numbers listed",
      "reason_for_recall": "Various reciprocating and oscillating saw blades were incorrectly labeled. The labeling errors include: (1) The pouch says oscillating saw blade when it actually contains a reciprocating saw blade; (2) The box bar code date does not match the human readable expiration date; and (3) The label incorrectly states use with Zimmer/Synthes handset and not the Zimmer Universal Power System.",
      "recall_initiation_date": "20130402",
      "center_classification_date": "20130415",
      "termination_date": "20140715",
      "report_date": "20130424",
      "code_info": "Lots Numbers included in Recall:  1X311,01251,16325,15023,15024,1Y224,23326,0X401,26385,1Y174,  17151,0Y280,17150,22028,28114,19071,23372,23346,23504,23505,  25134,25341,2W223,2X105,26001,2W573,2W574,24348,25304,  25333,26068,26165,27015,27016,29392,PD4647"
    }
  ]
}