The Recall Desk

Manufacturer

Medline Industries, LP

351 recalls in our database name Medline Industries, LP 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.

301–325 of 351

  • HighFDA (Devices)·Z-0519-2026·2025-11-26

    Medline Surgical Kits Recalled for Unintended Smoke Pencil Activation

    Medline Industries recalls 4,214 surgical kits containing SafeAir Smoke Evacuation Pencils that may activate unexpectedly when powered on or fail to deactivate when buttons are released. The defect poses a risk during surgical procedures.

    Product
    MEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF, REF CDS983639K; 2) BREAST ABD, REF CDS984267J; 3) PLASTIC PACK, REF DYNJ00264M; 4) BREAST ABDOMINOPLASTY MZ PK-LF, REF DYNJ0428947L; 5) BREAST ABDOMINOPLASTY MB PK-LF, REF DYNJ0428947M; 6) AUGMENTATION #
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2026·2025-11-26

    SafeAir Smoke Evacuation Pencils in Medline Surgical Kits Recalled for Unintended Activation

    Medline is recalling 40,151 surgical kits nationwide containing SafeAir Smoke Evacuation Pencils that may activate without manual input or fail to deactivate. This expands a previous Stryker recall from October 2024.

    Product
    MEDLINE convenience kits labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, REF CDS780119V; 2) BASIC BACK CDS, REF CDS780147N; 3) INSTRUMENTED BACK CDS, REF CDS780148R; 4) NEURO-LAMI CDS, REF CDS780208I; 5) TOTAL HIP, REF CDS920027Y; 6) TOTAL KNEE, REF CDS940072Y; 7) TOTA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0514-2026·2025-11-26

    Medline surgical kits recalled for unintended smoke pencil activation

    Medline is recalling 142 surgical kits containing SafeAir Smoke Evacuation Pencils that may activate without manual input or fail to deactivate when buttons are released. The kits have been distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: 1) CENTRAL LINE PACK, REF DYNJ00281P; 2) FREE FLAP PACK, REF DYNJ68213C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0527-2026·2025-11-26

    Medline Surgical Kits with Defective Smoke Evacuation Pencils Recalled

    Medline Industries is recalling 570 surgical kits containing SafeAir Smoke Evacuation Pencils that may activate without user input when plugged in or remain active after buttons are released.

    Product
    MEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF, REF DYNJ0160684F; 2) MAJOR LITHOTOMY PACK-LF, REF DYNJ0425778O; 3) MINOR VAGINAL #76-RF, REF DYNJ27434R; 4) ABDOMINAL HYST PACK, REF DYNJ44848M; 5) DA VINCI HYSTERECTOMY, REF DYNJ44863Q; 6) VAGINA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2026·2025-11-26

    Medline SafeAir Smoke Evacuation Pencil Kits Recalled for Unintended Activation

    Medline Industries is recalling convenience kits containing SafeAir Smoke Evacuation Pencils that may activate without user input when plugged in or remain active after being switched off. The affected kits are distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: GP-LEEP PACK-LF, REF PHS396969004F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2026·2025-11-26

    Medline Port Insertion Kit Smoke Evacuation Pencil Recall

    Medline is recalling convenience kits containing SafeAir Smoke Evacuation Pencils that may activate without user input or fail to deactivate when powered on. The recall affects kits distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0526-2026·2025-11-26

    Medline Surgical Kits Recalled for Smoke Evacuation Pencil Activation Risk

    Medline is recalling 11,032 surgical kits containing SafeAir Smoke Evacuation Pencils due to a potential malfunction risk. The pencils may activate without user input when plugged into a power source or remain active after buttons are released.

    Product
    MEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS, REF CDS820075W; 2) C-SECTION, REF CDS984261J; 3) C-SECTION CDS, REF CDS985282F; 4) C-SECTION PACK, REF DYNJ02577D; 5) C-SECTION PACK-LF, REF DYNJ0536924U; 6) C-SECTION PACK-LF, REF DYNJ0551169V; 7) C-SECT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0524-2026·2025-11-26

    Medline Surgical Smoke Evacuation Pencils Recalled for Unintended Activation

    Medline Industries is recalling convenience kits containing SafeAir Smoke Evacuation Pencils due to potential unintended activation or failure to deactivate, affecting 2844 kits distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY CDS #34-RF, REF CDS920099S; 2) GYN LAPAROSCOPY CDS-LF, REF CDS983764J; 3) ROBOTIC, REF CDS984262N; 4) ROBOTIC, REF CDS984262P; 5) ROBOTIC UROLOGY-RF, REF DYNJ38844N; 6) DA VINCI PROSTATE/COLPOPEXY, REF DYNJ44864
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0515-2026·2025-11-26

    Medline Breast Biopsy Kits Recalled for Smoke Evacuation Pencil Malfunction

    Medline is recalling breast biopsy kits with SafeAir Smoke Evacuation Pencils that may activate without manual input when plugged in or remain active when buttons are released. The recall affects 301 units distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: 1) BREAST BIOPSY PACK-LF, REF DYNJ0160598C; 2) BIOPSY BREAST PACK, REF DYNJ65361A; 3) BREAST BIOPSY/MASTECTOMY, REF DYNJ908839A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0510-2026·2025-11-26

    Medline Sterile Eye Procedure Kits Recalled for Potentially Open Seals

    Medline is recalling sterile eye procedure kits because the pouch packaging may exhibit open seals. A total of 1,024 units distributed in Missouri are affected.

    Product
    MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0520-2026·2025-11-26

    Medline Smoke Evacuation Pencils Recalled for Unintended Activation Risk

    Medline Industries is recalling 1,921 convenience kits containing smoke evacuation pencils that may activate without user input or fail to deactivate when buttons are released. Affected kits were distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3) MAJOR BASIN PACK, REF DYNJ59816A; 4) OSC BASIN PACK, REF DYNJ68217A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2026·2025-11-26

    Medline surgical kits with SafeAir smoke evacuation pencils recalled for unintended activation

    Medline recalls 20,941 surgical kits with SafeAir Smoke Evacuation Pencils due to unintended activation risk. The pencils may activate without user input or remain active after buttons are released.

    Product
    MEDLINE convenience kits labeled as: 1) GENERAL LAPAROSCOPY, REF CDS930027W; 2) GENERAL MAJOR CDS, REF CDS980245X; 3) BASIC GENERAL CDS, REF CDS980566F; 4) TOTAL KNEE CDS, REF CDS982823R; 5) BASIC CDS, REF CDS982936U; 6) UPPER EXTREMITY CDS, REF CDS983907M; 7) MAJO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0512-2026·2025-11-26

    Medline Kits Recalled for Unintended Activation of Smoke Evacuation Pencils

    Medline is recalling CATH LAB PACEMAKER PACK convenience kits containing SafeAir Smoke Evacuation Pencils due to risk of unintended activation when powered on or failure to deactivate. No injuries have been reported.

    Product
    MEDLINE convenience kits labeled as: CATH LAB PACEMAKER PACK, REF DYNJ59818A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0513-2026·2025-11-26

    Medline Convenience Kits with Smoke Evacuation Pencils Recalled for Unintended Activation

    Medline is recalling 5,133 convenience kits containing SafeAir Smoke Evacuation Pencils that may activate without manual input or remain active after buttons are released. The nationwide recall includes surgical kits for cardiovascular and other procedures.

    Product
    MEDLINE convenience kits labeled as: 1) GENERAL AAA #11-RF, REF CDS840261AB; 2) CAROTID ENDARTERECTOMY CDS-LF, REF CDS983637I; 3) PERIPHERAL VASCULAR CDS, REF CDS983723J; 4) ACH OPEN HEART, REF CDS983773J; 5) VASCULAR, REF CDS984255K; 6) OPEN HEART CHILDRENS PACK-LF,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0511-2026·2025-11-26

    MEDLINE Smoke Evacuation Pencil Kits Recalled for Unintended Activation Risk

    Medline is recalling specific convenience kits containing SafeAir Smoke Evacuation Pencils because they may activate without manual input or remain active after button release, posing a risk to surgical personnel.

    Product
    MEDLINE convenience kits labeled as LOCAL BASIC, REF DYNJ34418M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0516-2026·2025-11-26

    Medline Surgical and ENT Convenience Kits Recalled for Unexpected Activation Risk

    Medline Industries is recalling 3,078 surgical convenience kits containing SafeAir Smoke Evacuation Pencils. The devices may activate unexpectedly when plugged in or remain active after buttons are released.

    Product
    MEDLINE convenience kits labeled as: 1) HEAD AND NECK, REF CDS984259O; 2) HEAD AND NECK, REF CDS984259P; 3) MINOR ENT HARPER PACK-LF, REF DYNJ0160700F; 4) MAJOR ENT HARPER PACK-LF, REF DYNJ0161710I; 5) THORACOTOMY HARPER PACK-LF, REF DYNJ0161795F; 6) MAJOR ENT MZ PAC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0529-2026·2025-11-26

    Medline Smoke Evacuation Pencils Recalled for Unintended Activation Risk

    Medline Industries is recalling 345 convenience kits containing SafeAir Smoke Evacuation Pencils due to a potential for unintended activation or failure to deactivate. No injuries have been reported.

    Product
    MEDLINE convenience kits labeled as: 1) MINOR EYE TRAY #81, REF DYNJ27466S; 2) MINOR EYE TRAY #81, REF DYNJ27466T.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0522-2026·2025-11-26

    Medline Surgical Kits with SafeAir Pencils Recalled for Unintended Activation

    Medline is recalling specific kits containing SafeAir Smoke Evacuation Pencils that may activate without user input or remain active after buttons are released, posing a risk during surgical procedures.

    Product
    MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK, REF CDS780202R; 2) ACDF CDS, REF CDS941061M; 3) NEURO PACK-LF, REF DYNJ0038440C; 4) NEURO VP SHUNT/VAGAL NERVE-RF, REF DYNJ21925S; 5) NEURO-ORTHO EXTRAS, REF DYNJ44882M; 6) LAMINECTOMY, REF DYNJ903870F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0451-2026·2025-11-19

    Anesthesia circuit kits recalled for tubing cracks causing inadequate anesthetic delivery

    Medline Industries is recalling 96,406 anesthesia circuit convenience kits due to cracks in the expandable tubing. The cracks can cause anesthesia leaks, leading to hypoxia, hypoventilation, and inadequate anesthetic delivery, potentially resulting in serious injury or death.

    Product
    Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0447-2026·2025-11-19

    Anesthesia Circuit Tubing Cracks May Cause Hypoxia in Surgical Kits

    Medline breast hernia surgical kits may develop tubing cracks that cause anesthesia leaks, potentially leading to dangerous breathing complications or death. Multiple complaints have been received.

    Product
    Convenience Kit, BREAST HERNIA DYNJ909125G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0444-2026·2025-11-19

    Medline Anesthesia Circuit Kits Recalled for Tubing Cracks and Leak Risk

    Medline is recalling anesthesia circuit kits due to cracks in expandable tubing that can cause leaks, potentially resulting in hypoxia and inadequate anesthetic delivery to patients. The recall affects 96,406 units distributed nationwide and internationally.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0446-2026·2025-11-19

    Medline anesthesia tubing recalled due to cracks causing circuit leaks

    Medline Industries is recalling 96,406 anesthesia circuit tubing units due to cracks causing leaks that may lead to hypoxia and inadequate anesthetic delivery.

    Product
    DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D GENERAL LAPAROSCOPY-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0449-2026·2025-11-19

    Anesthesia Circuit Kits Recalled Due to Tubing Cracks Causing Leaks

    Medline Industries is recalling 96,406 anesthesia circuit kits due to cracks in expandable tubing that cause leaks, potentially resulting in hypoxia and inadequate anesthetic delivery.

    Product
    Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0442-2026·2025-11-19

    Medline anesthesia circuit kits recalled for cracked tubing and gas leaks

    Medline has recalled anesthesia circuit kits due to cracks in the 120-inch expandable tubing. Leaks can cause hypoxia, inadequate anesthetic delivery, and serious injury or death.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers: ADULT 120 EXPANDABLE W/MASK DYNJAA10591; ANES CIRC 120IN EXP-LF DYNJAA6555G; ANES CIRCUIT ADULT 120"-LF DYNJAA10817; ANESTHESIA 120" ADLT-LF DYNJAA10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0445-2026·2025-11-19

    Anesthesia Circuit Kits recalled due to tubing cracks and leaks

    Medline is recalling anesthesia circuit kits due to cracks in expandable tubing that cause leaks. These leaks may result in hypoxia, inadequate ventilation, and improper anesthetic delivery, potentially causing serious injury or death.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I; LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D
    Category
    Medical Device
    Distribution
    Distributed nationwide