{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86598",
      "recalling_firm": "Primus Corporation",
      "address_1": "4231 E 75th Ter",
      "address_2": "N/A",
      "postal_code": "64132-2059",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US - Arizona, California, District of Columbia, Florida, Georgia, Illinois, Louisiana, Massachusetts,  Michigan, Missouri, Nebraska, New Jersey, Nevada, New York, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia, Wisconsin  OUS - Bahrain, Iran, Malaysia, Saudi Arabia, Taiwan, Turkey, UAE, UK, Vietnam",
      "recall_number": "Z-0321-2021",
      "product_description": "Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation",
      "product_quantity": "97 devices (USA only)",
      "reason_for_recall": "The product did not receive pre-market approval or clearance.",
      "recall_initiation_date": "20201009",
      "center_classification_date": "20201031",
      "termination_date": "20211104",
      "report_date": "20201111",
      "code_info": "Product Name and Product Code    ultra2 Resolution Variants Analyzer / 03-01-0047  ultra2 Resolution Analytical Column / 01-05-0011  Resolution Analytical Column /  01-05-0015  FASC Position Marker / 01-04-0042  A2+F Control Material Kit / 01-04-0043  Mobile Phase 1 Reagent 3.8L / 01-03-0040  Mobile Phase 1 Reagent 940mL / 01-03-0042  Mobile Phase 2 Reagent 3.8L / 01-03-0041  Mobile Phase 2 Reagent 940mL / 01-03-0044  2 Diluent Reagent 3.8L / 01-03-0056  2 Diluent Reagent 940mL / 01-03-0059  System Wash Reagent / 01-03-0035    Analyzer Unit serial numbers:  100242 100314 100331 100354 100468 100541 100638 100746  100243 100316 100332 100355 100485 100551 100639 100747  100244 100317 100334 100356 100492 100558 100644 100751  100245 100319 100335 100357 100501 100559 100645 100758  100300 100321 100337 100358 100503 100561 100654 100765  100301 100322 100338 100359 100507 100562 100660 100802  100304 100323 100342 100360 100508 100563 100664   100305 100324 100343 100361 100510 100572 100666   100306 100325 100344 100404 100515 100574 100683   100309 100326 100345 100411 100518 100587 100729   100310 100327 100348 100416 100527 100590 100730   100312 100329 100351 100427 100531 100627 100743   100313 100330 100353 100446 100533 100633 100745"
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}