{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Anaheim",
      "address_1": "4225 E La Palma Ave",
      "reason_for_recall": "Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height at which the patient can be loaded/unloaded.",
      "address_2": "",
      "product_quantity": "81 US Distribution",
      "code_info": "Lot Code:  0086  0088  0024  0054  0056  0031  0040  0085  0046  0051  0121  0042  0032  0036  0021  0022  0015  0020  0065  0074  0066  0069  0007  0017  0005  0018  0004  0008  0062  0063  0038  0043  0033  0035  0037  0058  0071  0010  0011  0019  0049  0050  0055  0023  0039  0045  0059  0064  0028  0041  0044  0025  0001  0014  0068  0073  0057  0060  0027  0029  0030  0082  0083  0048  0070  0072  0034  0047  0009  0013  0080  0002  0081  0090  0091      Item No.  21762-135-33HJ  21762-135-33HJ  21762-135-33HJ  21762-135-33HJ  21762-135-33HJ  21762-110-36H",
      "center_classification_date": "20150630",
      "distribution_pattern": "US Distribution and Internationally to Japan and Jordan.",
      "state": "CA",
      "product_description": "Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-010-36H, 21762-010-41H,  21762-111-36H.",
      "report_date": "20150708",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sechrist Industries Inc",
      "recall_number": "Z-1939-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71455",
      "termination_date": "20151020",
      "more_code_info": "",
      "recall_initiation_date": "20150601",
      "postal_code": "92807-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}