The Recall Desk

Manufacturer

Medline Industries, LP

576 recalls in our database name Medline Industries, LP as the manufacturing or recalling firm.

What the numbers show

Total
576
Critical
36
Severe
104
Most recent
2026-10-21

Of the 576 recalls from Medline Industries, LP we have scored against our rubric, 36 (6%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 104 (18%) are Severe.

Which agencies issued them

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.

26–50 of 576

  • HighFDA (Devices)·Z-3230-2026·2026-09-30

    Medline Instrument Channel Brush Kits Recalled for Sharp Edges

    Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.

    Product
    Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3268-2026·2026-09-30

    Medline Neurological Surgery Kits Recalled for Endotoxin Variability

    Medline is recalling 234 neurological surgery kits nationwide due to potential endotoxin variability that may cause adverse health reactions.

    Product
    Medline Convenience Kits: 1) MAJOR NEURO VCH, Catalog Number: DYNJ39218I; 2) NEURO PACK-LF, Catalog Number: DYNJ41246F; 3) CRANIOTOMY PACK (CRSJE)227-LF, Catalog Number: DYNJ47487A; 4) MAJOR NEURO PACK, Catalog Number: DYNJ57233J; 5) NEURO, Catalog Number: DYNJ82388A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3267-2026·2026-09-30

    Medline Craniotomy Kits Recalled for Potential Endotoxin Variability

    Medline is recalling 486 craniotomy convenience kits due to potential endotoxin variability that may cause adverse health reactions.

    Product
    Medline Convenience Kits: 1) MFC CRANIOTOMY PACK, Catalog Number: DYNJT8784; 2) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348Q; 3) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348R; 4) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348S; 5) SLUH CRANIOTOMY…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3265-2026·2026-09-30

    Medline Neurological Sponges Recalled for Potential Endotoxin Variability

    Medline is recalling 695 convenience kits containing neurological sponges due to potential endotoxin variability that may cause adverse health reactions.

    Product
    Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Number: DYNJ02516G; 2) SINUS PACK-LF, Catalog Number: DYNJ0342705J; 3) NASAL-LF, Catalog Number: DYNJ40094G; 4) ENT PACK, Catalog Number: DYNJ50699F; 5) EENT PACK, Catalog Number: DYNJ83219
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3269-2026·2026-09-30

    Medline Neurological Surgery Kits Recalled for Endotoxin Variability

    Medline Industries is recalling 4,013 neurological surgery kits due to potential endotoxin variability that may cause adverse health reactions.

    Product
    Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3) CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348O; 4) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348P; 5) LAMINECTOMY PACK-LF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3125-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline Industries is recalling specific lots of Convenience Kits due to potential fungal contamination that could lead to serious adverse health consequences.

    Product
    Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3122-2026·2026-09-23

    Medline Convenience Kits Recalled for Potential Fungal Contamination

    Medline is recalling 489 convenience kits nationwide because they may contain sterile applicators contaminated with Aspergillus penicillioides, which can cause serious infection.

    Product
    Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Number: DYNDA1080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3127-2026·2026-09-23

    Medline Recalls Blood and Urine Collection Kits Due to Fungal Contamination

    Medline is recalling 47,848 blood and urine collection kits nationwide because they may contain Aspergillus penicillioides, a fungus that can cause serious infection.

    Product
    Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3) DYNDH1619A, Catalog Number: DYNDH1619A; 4) DYNDH1620A, Catalog Number: DYNDH1620A; 5) DYNDH1694A, Catalog Number: DYNDH1694A; 6) DYNDH1695, Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3126-2026·2026-09-23

    Medline Convenience Kits Recalled for Potential Fungal Contamination

    Medline Industries is recalling 1,100 convenience kits nationwide due to potential Aspergillus penicillioides contamination in sterile applicators.

    Product
    Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3121-2026·2026-09-23

    Medline Anesthesia Kits Recalled for Fungal Contamination Risk

    Medline is recalling specific lots of Anesthesia L&D A-Line Sets due to potential Aspergillus penicillioides contamination in sterile applicators.

    Product
    Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3123-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline Industries is recalling 447 convenience kits nationwide due to potential fungal contamination that could cause serious health consequences.

    Product
    Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3124-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline is recalling 10,407 convenience kits containing sterile applicators that may be contaminated with Aspergillus penicillioides, posing a risk of serious infection.

    Product
    Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog Number: ACC010726A; 5) DYNDB3061, Catalog Number: DYNDB3061; 6) DYNDH1245, Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3207-2026·2026-09-23

    Medline Anesthesia Pain Kits Recalled for Potential Sterility Compromise

    Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.

    Product
    Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3208-2026·2026-09-23

    Medline Recalls Minor Pack Convenience Kits Due to Open Sterile Seals

    Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.

    Product
    Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3137-2026·2026-09-23

    Medline Open Heart A Pack Kits Recalled for Sterility Concerns

    Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.

    Product
    Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3209-2026·2026-09-23

    Medline Myringotomy Kits Recalled for Potential Sterility Compromise

    Medline Industries is recalling 60 Myringotomy Pack-LF kits due to open seals that may compromise sterility and lead to patient infection.

    Product
    Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3210-2026·2026-09-23

    Medline Recalls Cataract Convenience Kits Due to Open Sterile Seals

    Medline Industries is recalling 336 cataract convenience kits because open sterile seals may compromise sterility and lead to patient infection.

    Product
    Convenience kits CATARACT PACK DYNJ59881A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3061-2026·2026-09-09

    Medline Eye and Cataract Kits Recalled for Potential Sterility Breach

    Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3063-2026·2026-09-09

    Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach

    Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3062-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3048-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3057-2026·2026-09-09

    Medline Blood Culture Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3060-2026·2026-09-09

    Medline C-Section Prep Kits Recalled for Potential Sterility Breach

    Medline is recalling 352 C-Section Prep kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) C-SECTION PREP, Model Number: DYNJ32702B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3053-2026·2026-09-09

    Medline Ultrasound Breast Pack Recalled for Potential Sterility Breach

    Medline is recalling 300 Ultrasound Breast Packs due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3059-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.

    Product
    Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
    Category
    Medical Device
    Distribution
    Distributed nationwide