The Recall Desk

Manufacturer

MEDLINE INDUSTRIES, LP - Northfield

787 recalls in our database name MEDLINE INDUSTRIES, LP - Northfield as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–25 of 787

  • SevereFDA (Devices)·Z-2567-2025·2025-10-01

    Medline Medical Convenience Kits with Defective Laryngoscope Handles

    Medline Industries is recalling specific medical convenience kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles because the light fails to illuminate as intended, potentially affecting resuscitation and airway management procedures.

    Product
    Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number ACC010671; 4. DRAWER #2, Kit Number ACC010728.
    Category
    Medical Device
    Distribution
    6 states
  • Severity pendingFDA (Devices)·Z-2566-2025·2025-10-01

    Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2

    Pending LLM rewrite. Source: FDA_DEVICE Z-2566-2025.

    Product
    Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number ACC010392; 4. INTUBATION KIT, Kit Number ACC010467A; 5. ADULT AIRWAY TRAY, Kit Number ACC01
    Category
    Medical Device
    Distribution
    6 states
  • Severity pendingFDA (Devices)·Z-2452-2025·2025-09-03

    The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care

    Pending LLM rewrite. Source: FDA_DEVICE Z-2452-2025.

    Product
    The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of components dependent upon the specific procedure. These kits will be assembled using
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Drugs)·D-0600-2025·2025-09-03

    MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)

    Pending LLM rewrite. Source: FDA_DRUG D-0600-2025.

    Product
    MEDLINE ALCOHOL PREP — MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Drugs)·D-0601-2025·2025-09-03

    CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)

    Pending LLM rewrite. Source: FDA_DRUG D-0601-2025.

    Product
    CURAD ALCOHOL PREP PADS — CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-2479-2025·2025-09-03

    Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTI

    Pending LLM rewrite. Source: FDA_DEVICE Z-2479-2025.

    Product
    Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only units from SKU DYNJG001004A LAVH MINOR were distributed)
    Category
    Medical Device
    Distribution
    2 states
  • Severity pendingFDA (Devices)·Z-2460-2025·2025-09-03

    Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Cathe

    Pending LLM rewrite. Source: FDA_DEVICE Z-2460-2025.

    Product
    Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH, 401210RH, 401211RH, 401212RH, 401222RH, 401223RH, 401226RH, 401227RH, 401228RH, 401260RH, 401261RH, 401271RH, 401305RH, 401306RH, 401309RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Drugs)·D-0603-2025·2025-09-03

    INCONTROL ALCOHOL (ISOPROPYL ALCOHOL)

    Pending LLM rewrite. Source: FDA_DRUG D-0603-2025.

    Product
    INCONTROL ALCOHOL — INCONTROL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Drugs)·D-0605-2025·2025-09-03

    ALCOHOL (ISOPROPYL ALCOHOL)

    Pending LLM rewrite. Source: FDA_DRUG D-0605-2025.

    Product
    ALCOHOL — ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Drugs)·D-0602-2025·2025-09-03

    WALMART (ISOPROPYL ALCOHOL)

    Pending LLM rewrite. Source: FDA_DRUG D-0602-2025.

    Product
    WALMART — WALMART (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2043-2025·2025-07-09

    Medline IV Catheters Recalled for Needle Retraction Failure

    Medline Industries is recalling specific Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters because the needle may be slow to retract or fail to retract during catheter insertion.

    Product
    Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1995-2025·2025-07-02

    Medline Umbilical Tray sterile packaging defect recall

    Medline is recalling umbilical trays due to a possible packaging defect in the outer Tyvec pouch that protects the sterile product. The defect may compromise sterility.

    Product
    Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1810-2025·2025-06-11

    Medline Craniotomy Kits with Defective Codman Disposable Perforators

    Medline is recalling craniotomy kits containing Codman Disposable Perforators with inadequate welds that may break or separate during use.

    Product
    Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-1809-2025·2025-06-11

    Medline Surgical Kits with Codman Disposable Perforator recalled

    Medline surgical kits containing Codman Disposable Perforators are being recalled because certain lots have inadequate welds that may cause the perforator to break or separate during use.

    Product
    Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS983611N 3. CRANIOTOMY CDS, SKU CDS983467J 4. CRANIOTOMY PACK, SKU DYNJ85807A, DYNJ85927 5. MAJOR CRANIOTOMY PACK, SKU DYNJ82007A
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-1811-2025·2025-06-11

    Medline Craniotomy Kits with Defective Codman Disposable Perforators Recalled

    Medline is recalling multiple craniotomy kits containing Codman Disposable Perforators due to inadequate welds that may cause the perforators to break or separate during use.

    Product
    Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ACCESSORY PACK SKU DYNJ59270 2. CRANI PACK-LF SKU DYNJ44805M 3. CRANIOTOMY SKU CDS982719V CDS982719W DYNJ904168F DYNJ908404B DYNJ908723A DYNJ908723C 4. CRANIOTOMY #IMF 56646-LF SKU DYN
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-1766-2025·2025-05-21

    Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk

    Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.

    Product
    Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1765-2025·2025-05-21

    Centurion Sterile Weitlaner Retractor recalled for packaging puncture risk

    Medline Industries is recalling Centurion Sterile Weitlaner Retractors (2,100 units) due to potential puncture damage to sterile packaging. The defect could compromise the sterility of the surgical instrument.

    Product
    Centurion Sterile Weitlaner Retractor, Reorder: 67315
    Category
    Medical Device
    Distribution
    Distributed nationwide