{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "28552",
      "product_res_number": "Z-0051-04",
      "event_date_initiated": "2002-08-09",
      "event_date_posted": "2003-10-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-10-23",
      "res_event_number": "26844",
      "product_code": "G-IO",
      "product_description": "propper brand cal-mark(R),  Micro-Hematocrit Calibrated Capillary Tubes, CALIBRATED-HEPARINIZED, reorder no. 043021, 6 Vials, 100 Tubes per Vial, Length 75 mm., 0.55 mm. I.D., 1.40-1.75mm. O.D. \n\nCalibrated 60mm from end for use in direct reading centrifuges. Fill to the 60mm mark with blood and seal opposite end by flame or with sealing compound.  If centrifuged on a direct reading centrifuge, read percent hematocrit directly from scale on the centrifuge.  Otherwise, read in normal manner as a percent ratio of packed cells with 60mm of sample as 100%. \n\nFirm on label: propper manufacturing co., inc., long island city, n.y. 11101.",
      "code_info": "Reorder No. 043021,  Lot # C0402",
      "firm_fei_number": "2410251",
      "recalling_firm": "Propper Mfg Co Inc",
      "address_1": "36-04 Skillman Avenue",
      "city": "City",
      "state": "NY",
      "postal_code": "11101",
      "additional_info_contact": "Frank E. Platko\n718-392-6650",
      "reason_for_recall": "Deviation in capillary tubes could cause a 10% increase in read out values which could make a slight anemic patient appear to have a normal reading.",
      "root_cause_description": "Other",
      "action": "On 8/9/02, Propper faxed a 'Request for Return' of the  product to the consignees advising them of the problem and that a replacement will be sent for all returned product.  On 11/27/02, Propper faxed a second 'Request for Return of Product' to its consignees.  The firm destroyed the recovered and held stock.",
      "product_quantity": "178 boxes",
      "distribution_pattern": "Distributors located in TX, UT, ID, IL, IA, IN, MN, WI, OH, CT, MO, PA, VA.",
      "openfda": {}
    }
  ]
}