{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "96282",
      "product_res_number": "Z-0894-2011",
      "event_date_initiated": "2010-12-06",
      "event_date_posted": "2011-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-07-05",
      "res_event_number": "57463",
      "product_code": "OFM",
      "product_description": "Blood Center Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use, Reorder No. Q921CL, Manufactured for : Blood Center of Wisconsin, Milwaukee, WI. \n\nPort VAD Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use, Reorder No. 3540CL, Manufactured for : McCormick Medical Distribution, Edmonds, WA 98020.\nThe kits are used by blood centers to draw blood.",
      "code_info": "Lot 912024, 1004229, 1007091 (Reorder # Q921CL) Lot 1001066 (Reorder # 3540CL)",
      "firm_fei_number": "2128604",
      "recalling_firm": "Continental Medical Labs,Inc",
      "address_1": "813 Ela Ave / PO Box 306 813 Ela Ave /",
      "address_2": "PO Box 306",
      "city": "Waterford",
      "state": "WI",
      "postal_code": "53185-0306",
      "additional_info_contact": "414-534-2787",
      "reason_for_recall": "Continental Medical labs, Inc,  is recalling various  lots of Blood Center Kit and Port VAD Kits  because Covidien reported that  testing could not pick up an Over-Sulfated Chondroitin Sulfate (OSCS) contaminant in the purified heparin sodium USP.",
      "root_cause_description": "Material/Component Contamination",
      "action": "Covidien sent an URGENT PRODUCT RECALL letter dated November 12, 2010, to their distributors.  \nContinental Medical Labs,Inc telephoned on 12/06/2010 and later sent a letter dated December 7, 2010, with an enclosed copy of the recall notice.  The letters were addressed to McCormick Medical Distribution, Inc and to Medico Mart, Inc.  The letter described the problem and product affected. Advised consignees to inform all their customers to return the product as well as the distribution information as soon as possible so CML could notify Covidien for replacements.\nFor questions regarding this recall call (262) 723-6715, ext. 313.",
      "product_quantity": "30 cases, 30 kits per case",
      "distribution_pattern": "Nationwide Distribution including WA and WI",
      "openfda": {
        "device_name": "Phlebotomy Blood Collection Kit",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2750",
        "device_class": "2",
        "registration_number": [
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