{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "345 E Main St",
      "reason_for_recall": "Lot specific  Trabecular Metal (TM) Reverse Shoulder Liner Impactors are being recalled due to reports  of alignment peg fractures. All lots of TM Reverse Shoulder Liner Impactors manufactured from 455 stainless steel are being retrieved, as all reported fractured instruments were manufactured with this  material. The TM Reverse Shoulder Liner Impactor units that were manufactured with 13-8  stain",
      "address_2": "",
      "product_quantity": "185 (162 in USA)",
      "code_info": "part 00-4309-028-00, lot 60443178, 60545332, 60549563, 60605851, 60612791, 60720047  60758647 60773944  60836577  60896973,  60973522,  61019783,  61024158",
      "center_classification_date": "20120816",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and internationally to Germany, Belgium, Denmark, Finland, France, Italy, Netherlands, Spain, Sweden, Switzerland, and the United Kingdom.",
      "state": "IN",
      "product_description": "Trabecular Metal Reverse Shoulder Liner 40mm, part 00-4309-028-00 -     Per surgical technique 97-4309-003-00 Revision 4: \"Complete Poly Liner insertion by snapping the appropriate 60¿ (Standard) or 65¿ (Retentive) Poly Liner Impactor to the Poly Liner Impactor Handle. Then, place the Poly Liner Impactor on the Poly Liner articular surface and forcefully strike the Poly Liner Handle with a mallet.\"",
      "report_date": "20120822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-2212-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "62540",
      "termination_date": "20140417",
      "more_code_info": "",
      "recall_initiation_date": "20120718",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}