{
  "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": "188910",
      "product_res_number": "Z-0030-2022",
      "event_date_initiated": "2021-07-27",
      "event_date_created": "2021-10-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-06-07",
      "res_event_number": "88529",
      "product_code": "MRC",
      "k_numbers": [
        "K181566"
      ],
      "product_description": "Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002",
      "code_info": "Lot Number: FOE",
      "firm_fei_number": "3016114779",
      "recalling_firm": "Contamac Solutions, Inc.",
      "address_1": "806 Kimball Ave",
      "city": "Grand Junction",
      "state": "CO",
      "postal_code": "81501-3842",
      "additional_info_contact": "Contamac Customer Service\n833-266-8262",
      "reason_for_recall": "Contact lens solution may contain foreign material",
      "root_cause_description": "Device Design",
      "action": "On 8/5/2021, Contamac, issued a \"Urgent: Medical Device recall\" notification to affected consignees. In addition to informing consignees about the recall product, Contamac asked consignees to take the following actions:\n\n 1.\tRefer to the package label and Product Distribution Information below to verify the product is impacted (i.e. lot FOE).\n\n2.\tImmediately discontinue use of impacted product\n\n3.\tDestroy and discard the product (i.e. remove vial cap and empty contents before discarding)\n\n4.\tNotify us using the following link to confirm that you received this recall notification and have discarded impacted product: Customer Form\n\n5. If you have questions, please contact Toll-Free: 1-833-266-8262, Telephone: 1-970-985-4240, E-Mail: hello@nutrifill.com, Hours: M-F 9:00 am - 5:00 pm MDT\n\n6. Adverse reactions or quality problems experienced with the use of this product may be reported to FDA:\n\tOnline at https://www.accessdata.fda.gov/scripts/medwatch/index.cfm or,\n\tCall FDA 1-800-FDA-1088",
      "product_quantity": "104335 vials",
      "distribution_pattern": "US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY.\n\nOUS: N/A",
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          "K983836",
          "K122273",
          "K000385",
          "K181566",
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        ],
        "device_name": "Products, Contact Lens Care, Rigid Gas Permeable",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5918",
        "device_class": "2",
        "registration_number": [
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}