{
  "companyId": "63111",
  "slug": "medline-industries-lp-63111",
  "name": "Medline Industries, LP",
  "clearances": {
    "total": 267,
    "last12Months": 5,
    "first": "1977-01-05",
    "latest": "2026-06-22"
  },
  "medianReviewDays": 116,
  "productCodeCount": 107,
  "recalls": {
    "total": 616,
    "openLast12Months": 473,
    "recent": [
      {
        "resNumber": "Z-2788-2026",
        "productCode": "OEZ",
        "status": "Open, Classified",
        "recallClass": "Class II",
        "initiated": "2026-06-11",
        "reason": "Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species."
      },
      {
        "resNumber": "Z-2789-2026",
        "productCode": "LRO",
        "status": "Open, Classified",
        "recallClass": "Class II",
        "initiated": "2026-06-11",
        "reason": "Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species."
      },
      {
        "resNumber": "Z-2790-2026",
        "productCode": "OJG",
        "status": "Open, Classified",
        "recallClass": "Class II",
        "initiated": "2026-06-11",
        "reason": "Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species."
      },
      {
        "resNumber": "Z-2791-2026",
        "productCode": "OJH",
        "status": "Open, Classified",
        "recallClass": "Class II",
        "initiated": "2026-06-11",
        "reason": "Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species."
      },
      {
        "resNumber": "Z-2736-2026",
        "productCode": "LRO",
        "status": "Open, Classified",
        "recallClass": "Class II",
        "initiated": "2026-06-10",
        "reason": "Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to find another readily available device."
      }
    ]
  },
  "registration": {
    "sites": 2,
    "countries": [
      "US"
    ]
  },
  "productCodes": [
    {
      "code": "FYA",
      "deviceName": "Gown, Surgical",
      "clearances": 16,
      "latest": "2025-02-26",
      "medianReviewDays": 126
    },
    {
      "code": "LZA",
      "deviceName": "Polymer Patient Examination Glove",
      "clearances": 13,
      "latest": "2020-10-26",
      "medianReviewDays": 137
    },
    {
      "code": "KGO",
      "deviceName": "Surgeon'S Gloves",
      "clearances": 12,
      "latest": "2021-08-02",
      "medianReviewDays": 150
    },
    {
      "code": "FRG",
      "deviceName": "Wrap, Sterilization",
      "clearances": 11,
      "latest": "2024-09-17",
      "medianReviewDays": 240
    },
    {
      "code": "FRO",
      "deviceName": "Dressing, Wound, Drug",
      "clearances": 9,
      "latest": "2024-03-26",
      "medianReviewDays": 181
    },
    {
      "code": "INI",
      "deviceName": "Vehicle, Motorized 3-Wheeled",
      "clearances": 9,
      "latest": "2004-10-08",
      "medianReviewDays": 32
    },
    {
      "code": "GEI",
      "deviceName": "Electrosurgical, Cutting & Coagulation & Accessories",
      "clearances": 8,
      "latest": "2024-12-19",
      "medianReviewDays": 109
    },
    {
      "code": "LYY",
      "deviceName": "Latex Patient Examination Glove",
      "clearances": 8,
      "latest": "2011-04-21",
      "medianReviewDays": 102
    },
    {
      "code": "HRS",
      "deviceName": "Plate, Fixation, Bone",
      "clearances": 6,
      "latest": "2023-01-25",
      "medianReviewDays": 113
    },
    {
      "code": "KKX",
      "deviceName": "Drape, Surgical, Antimicrobial",
      "clearances": 6,
      "latest": "2006-02-15",
      "medianReviewDays": 132
    },
    {
      "code": "FMQ",
      "deviceName": "Restraint, Protective",
      "clearances": 5,
      "latest": "1996-10-29",
      "medianReviewDays": 53
    },
    {
      "code": "HWC",
      "deviceName": "Screw, Fixation, Bone",
      "clearances": 5,
      "latest": "2024-08-02",
      "medianReviewDays": 80
    },
    {
      "code": "KNT",
      "deviceName": "Tubes, Gastrointestinal (And Accessories)",
      "clearances": 5,
      "latest": "2019-05-04",
      "medianReviewDays": 46
    },
    {
      "code": "KOD",
      "deviceName": "Catheter, Urological",
      "clearances": 5,
      "latest": "1984-05-09",
      "medianReviewDays": 20
    },
    {
      "code": "LRO",
      "deviceName": "General Surgery Tray",
      "clearances": 5,
      "latest": "2022-05-24",
      "medianReviewDays": 136
    },
    {
      "code": "LYZ",
      "deviceName": "Vinyl Patient Examination Glove",
      "clearances": 5,
      "latest": "2020-10-26",
      "medianReviewDays": 83
    },
    {
      "code": "BTT",
      "deviceName": "Humidifier, Respiratory Gas, (Direct Patient Interface)",
      "clearances": 4,
      "latest": "2025-07-02",
      "medianReviewDays": 182
    },
    {
      "code": "FMF",
      "deviceName": "Syringe, Piston",
      "clearances": 4,
      "latest": "2024-02-16",
      "medianReviewDays": 72
    },
    {
      "code": "JDR",
      "deviceName": "Staple, Fixation, Bone",
      "clearances": 4,
      "latest": "2025-04-11",
      "medianReviewDays": 43
    },
    {
      "code": "KNX",
      "deviceName": "Collector, Urine, (And Accessories) For Indwelling Catheter",
      "clearances": 4,
      "latest": "1997-12-11",
      "medianReviewDays": 56
    },
    {
      "code": "CAF",
      "deviceName": "Nebulizer (Direct Patient Interface)",
      "clearances": 3,
      "latest": "2024-01-04",
      "medianReviewDays": 266
    },
    {
      "code": "DQO",
      "deviceName": "Catheter, Intravascular, Diagnostic",
      "clearances": 3,
      "latest": "2017-01-19",
      "medianReviewDays": 294
    },
    {
      "code": "DXQ",
      "deviceName": "Blood Pressure Cuff",
      "clearances": 3,
      "latest": "2026-06-22",
      "medianReviewDays": 173
    },
    {
      "code": "EZL",
      "deviceName": "Catheter, Retention Type, Balloon",
      "clearances": 3,
      "latest": "2015-01-09",
      "medianReviewDays": 114
    },
    {
      "code": "FLL",
      "deviceName": "Continuous Measurement Thermometer",
      "clearances": 3,
      "latest": "2021-09-20",
      "medianReviewDays": 110
    }
  ],
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  "productCodesTotal": "107",
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    {
      "kNumber": "K254287",
      "deviceName": "Medline Reusable Blood Pressure Cuff",
      "productCode": "DXQ",
      "decisionDate": "2026-06-22",
      "reviewDays": 173
    },
    {
      "kNumber": "K253322",
      "deviceName": "Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with 78 Infant Circuit, HUD99060KIT / Dri-Tech with 78 Infant Circuit Kit, HUD99001KIT / Single Limb Infant Circuit Dri-Tech Kit, HUD99009KIT / Dri-Tech with 60 Infant Circuit Kit, HUD99018KIT / Dri-Tech with 44 Infant Circuit Kit, HUD870NKIT / Dri-Tech Infant Accessory Bag, HUD1631 / Infant Wye Connector with Swivel)",
      "productCode": "BZE",
      "decisionDate": "2026-03-25",
      "reviewDays": 176
    },
    {
      "kNumber": "K251687",
      "deviceName": "Konig Bell Circumcision Clamp",
      "productCode": "HFX",
      "decisionDate": "2026-02-25",
      "reviewDays": 268
    },
    {
      "kNumber": "K253070",
      "deviceName": "Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)",
      "productCode": "DXC",
      "decisionDate": "2025-11-20",
      "reviewDays": 58
    },
    {
      "kNumber": "K250345",
      "deviceName": "Medline Bag Decanter",
      "productCode": "LHI",
      "decisionDate": "2025-10-24",
      "reviewDays": 260
    },
    {
      "kNumber": "K250312",
      "deviceName": "Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra Small",
      "productCode": "BTT",
      "decisionDate": "2025-07-02",
      "reviewDays": 149
    },
    {
      "kNumber": "K243888",
      "deviceName": "Medline UNITE®  REFLEX®  Hybrid Nitinol Implant System",
      "productCode": "JDR",
      "decisionDate": "2025-04-11",
      "reviewDays": 114
    },
    {
      "kNumber": "K242844",
      "deviceName": "Medline Level 4 Surgical Gown with Breathable Sleeves",
      "productCode": "FYA",
      "decisionDate": "2025-02-26",
      "reviewDays": 159
    },
    {
      "kNumber": "K242370",
      "deviceName": "Medline Microdissection Needle (4cm) (140936 (ESE104A)); Medline Microdissection Needle (3cm) (140937 (ESE103A))",
      "productCode": "GEI",
      "decisionDate": "2024-12-19",
      "reviewDays": 132
    },
    {
      "kNumber": "K241778",
      "deviceName": "Hudson RCI Comfort Flo® CubCannula",
      "productCode": "BTT",
      "decisionDate": "2024-12-19",
      "reviewDays": 182
    }
  ],
  "nameVariants": {
    "total": "13",
    "shown": [
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        "name": "MEDLINE INDUSTRIES INC",
        "dataset": "device/enforcement",
        "method": "normalised"
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      {
        "name": "MEDLINE INDUSTRIES INC",
        "dataset": "device/recall",
        "method": "normalised"
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      {
        "name": "Medline Industries Inc",
        "dataset": "device/enforcement",
        "method": "normalised"
      },
      {
        "name": "Medline Industries Inc",
        "dataset": "device/recall",
        "method": "normalised"
      },
      {
        "name": "Medline Industries Inc.",
        "dataset": "device/recall",
        "method": "normalised"
      },
      {
        "name": "Medline Industries Inc.",
        "dataset": "device/enforcement",
        "method": "normalised"
      },
      {
        "name": "Medline Industries, Inc.",
        "dataset": "device/510k",
        "method": "normalised"
      },
      {
        "name": "Medline Industries, Inc.",
        "dataset": "device/recall",
        "method": "normalised"
      }
    ]
  },
  "sources": {
    "clearances": "https://api.fda.gov/device/510k.json?search=applicant%3A%22Medline%20Industries%2C%20LP%22",
    "recalls": "https://api.fda.gov/device/recall.json?search=recalling_firm%3A%22Medline%20Industries%2C%20LP%22"
  },
  "provenance": [
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      "dataset": "device/510k",
      "loadedAt": "2026-08-10T19:40:09Z",
      "ingestRun": 51
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      "loadedAt": "2026-08-10T06:54:18Z",
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      "loadedAt": "2026-08-10T19:40:12Z",
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      "loadedAt": "2026-08-11T13:58:22Z",
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    },
    {
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      "loadedAt": "2026-08-10T19:40:11Z",
      "ingestRun": 52
    },
    {
      "dataset": "device/registrationlisting",
      "loadedAt": "2026-08-10T07:06:24Z",
      "ingestRun": 10
    }
  ],
  "retrievedAt": "2026-08-11T14:48:53.026Z"
}
