{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "48102",
      "product_res_number": "Z-0170-2007",
      "event_date_initiated": "2006-08-23",
      "event_date_posted": "2006-11-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-01-04",
      "res_event_number": "36160",
      "product_code": "MMK",
      "k_numbers": [
        "K931664",
        "K941664"
      ],
      "product_description": "5 Qt. Wallmount Sharps Container, Model 150, Regular Size; colors 202 Beige, 030 Red, 040 Yellow, 24 count containers; Made in USA for: Medline Industries; BEMIS label has Manufactured by Bemis Mtg. Co., Sheboygan Falls, WI.",
      "code_info": "BEMIS: Model 7H150 020 includes lot 20060001 to 20060016;  BEMiS: Model 7H150 030 includes lot 20050006, 20060001 to 20060008;  BEMIS: Model 7H150 040 includes lot 20060001 to 20060008;  Medline Model 7H950 030 includes lot 20050027, 20060001 to 20060008.",
      "firm_fei_number": "2126626",
      "recalling_firm": "Bemis Health Care,Inc",
      "address_1": "300 Mill St",
      "city": "Sheboygan Falls",
      "state": "WI",
      "postal_code": "53085-1807",
      "additional_info_contact": "Nancy Steinpreis\n920-467-5464",
      "reason_for_recall": "The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container.",
      "root_cause_description": "Other",
      "action": "Letters were mailed to consignees August 23, 2006 describing the product with lots and model numbers. Customers were asked to have product destroyed rather than returned to Bemis.   Enclosed with the letter was a Recall Acknowledgement/Destroy in field form that they were instructed to fax to BEMIS.   A second letter was sent out to the non-responders on September 13, 2005.",
      "product_quantity": "145,656 Units",
      "distribution_pattern": "Nationwide and Canada.",
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        "device_name": "Container, Sharps",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5570",
        "device_class": "2"
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}