{
  "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": "Allentown",
      "address_1": "2201 Hangar Pl",
      "reason_for_recall": "Complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.",
      "address_2": "Ste 200",
      "product_quantity": "64",
      "code_info": "All affected product in the U.S are from the same LOT #1402S, Model #s 6133-6136",
      "center_classification_date": "20150514",
      "distribution_pattern": "US Distribution to the states of : FL, CA, NJ, NC and MD.",
      "state": "PA",
      "product_description": "ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch.  Patient transfer aid.",
      "report_date": "20150520",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Handicare USA, Inc.",
      "recall_number": "Z-1613-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70995",
      "termination_date": "20150817",
      "more_code_info": "",
      "recall_initiation_date": "20150326",
      "postal_code": "18109-9342",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}