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RecallsAboutBlog

Medline Industries, LP

Medline Industries, LP: 59 recalls listed since January 2026 across FDA; 11 rated high risk.

By year

  • 202659

By agency

  • FDA59

By category

  • Medical Device59

All recalls (59)

Medline C-Section Drapes and Medical Convenience Kits

Medline C-Section Drapes and Medical Convenience Kits are difficult to remove from the patient and leave adhesive residue on the patient's skin.

Moderate risk, FDA, , Device defect

Medline Foot Ankle Convenience Kit

The Medline convenience kit labeled Foot Ankle has a discrepancy in the shelf-life of a component.

Moderate risk, FDA, , Device defect

Medline Convenience Kits Containing CONMED AirSeal Access Ports

Convenience Kits containing Conmed AirSeal Access Ports may cause delays or ending procedures due to erroneous overpressure alerts and system venting.

Moderate risk, FDA, , Device defect

Medline Surgical Convenience Kits

Medline surgical convenience kits contain cannula components that may leak or break during use.

Moderate risk, FDA, , Device defect

Medline Bariatric Steel Rollators

The rollator's front fork stem bolt/wheel assembly may disconnect, causing the front wheels to detach and risk severe falls.

Moderate risk, FDA, , Device defect

Medline Homecare Beds and Hand Pendants

Hand pendants for Medline homecare beds can overheat, posing a fire hazard.

High risk, FDA, , Device defect

Medline Convenience Kits

The kits contain neurological sponges with potential for unexpected variability of endotoxin levels.

Moderate risk, FDA, , Contamination

Medline Convenience Kits Containing Healthmark Instrument Channel Brushes

Medline convenience kits contain brushes with a sharp edge that can cut and infect.

Moderate risk, FDA, , Device defect

Medline Convenience Kits for Anesthesia, Minor Procedures, Myringotomy and Cataract Surgery

Convenience kits may have open seals in sterile pouch packaging, which can compromise sterility and lead to contamination or patient infection.

Moderate risk, FDA, , Sterility problem

Medline Convenience Kits

Medline Convenience Kits contain sterile applicators that may have fungal contamination, potentially causing serious infections.

High risk, FDA, , Contamination

Medline Open Heart A Pack Convenience Kit

The Medline Convenience Kit contains a cannula that may have a sterile barrier breach, risking infection.

Moderate risk, FDA, , Sterility problem

Medline Convenience Kits with BD ChloraPrep Applicators

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators may have an open or incomplete seal, leading to infection.

Moderate risk, FDA, , Contamination

Medline Convenience Kits

Medline Convenience Kits contain applicators with a potential breach of sterility in the packaging.

Moderate risk, FDA, , Sterility problem

Medline Convenience Kits

Medline convenience kits contain a potentially contaminated component.

Moderate risk, FDA, , Contamination

Medline Trach Tube Kit

The Medline medical convenience kit labeled as Trach Tube Kit has a component labeling discrepancy.

Moderate risk, FDA, , Labeling error

Medline Medical Convenience Kits

Medline medical convenience kits contain neurosponges with potential out-of-specification endotoxin levels.

Moderate risk, FDA, , Quality testing problem

Medline Micro-Kill Bleach Germicidal Bleach Wipes

Medline Micro-Kill Bleach Germicidal Bleach Wipes may have reduced bleach concentration before the end of their shelf life.

Moderate risk, FDA, , Contamination

Medline Hudson RCI Heated Neonatal Breathing Circuits

Neonatal and infant heated wire breathing circuits may experience sporadic failure.

Moderate risk, FDA, , Device defect

Medline Medical Convenience Kits

Medline medical convenience kits may be contaminated with low levels of Bacillus species.

Moderate risk, FDA, , Contamination

Medline Convenience Kits Containing Bard Silastic Foley Catheters

Medline convenience kits contain Bard Silastic Foley Catheters with increased raw material on the surface, which may be harmful.

Moderate risk, FDA, , Device defect

Medline Hip and Knee Procedure Kits

The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.

High risk, FDA, , Device defect

Medline Convenience Kits

Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.

High risk, FDA, , Device defect

Medline Kits Containing Zimmer Biomet Mixing Bowls and Spatulas

Medline kits with Zimmer Biomet mixing bowls and spatulas have seal nonconformities risking sterility breach.

Moderate risk, FDA, , Sterility problem

Medline Convenience Kits

Medline Convenience Kits contain temperature probes with an error in their distribution control process.

Moderate risk, FDA, , Device defect

Medline Reprocessed Electrophysiology and Ultrasound Catheters

Reprocessed electrophysiology catheters may contain small particles of residual material, posing a risk of inflammatory response or infection.

High risk, FDA, , Foreign object

Medline Convenience Kits

Medline Convenience Kits contain lidocaine ampules with quality issues that may affect their use.

Moderate risk, FDA, , Device defect

Medline Convenience Kits Containing Recalled Swan-Ganz Catheters

Medline Convenience kits contain Swan-Ganz catheters with leaks or breakage that may lead to infection, medication loss, or blood loss.

Moderate risk, FDA, , Device defect

Medline Convenience Kits with 10mL Polycarbonate Colored Syringes

Convenience kits with 10mL polycarbonate syringes have unapproved design changes.

Moderate risk, FDA, , Unapproved product

Medline Convenience Kits

Medline Convenience Kits contain lidocaine and bupivacaine injections with quality issues.

High risk, FDA, , Device defect

Medline Urethral Catheters and Procedure Kits

Medline urethral catheters and kits may have surface irregularities or connector issues.

Moderate risk, FDA, , Quality testing problem

Medline Convenience Kits

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive.

Moderate risk, FDA, , Device defect

Medline Eye Tray-LF Medical Convenience Kit

The Medline Eye Tray-LF kit contains syringes labeled as 1 mL but are U-100 insulin syringes.

Moderate risk, FDA, , Labeling error

Medline Anesthesia and Spinal Trays

Medline kits containing Huons Bupivacaine in Dextrose Injection have quality issues, including data integrity concerns and efficacy complaints.

High risk, FDA, , Device defect

Namic Manifolds and Kits

Namic Angiographic Manifolds contain particulate within the fluid path.

High risk, FDA, , Foreign object

Medline Convenience Kits, Surgical Drapes, Gowns and Packs

Medline Convenience Kits and Surgical Drapes may not be sterile due to calibration issues with sterilization equipment.

Moderate risk, FDA, , Sterility problem

Medline and Centurion Medical Convenience Kits

Medical convenience kits containing Webcol Large Alcohol Prep Pads may not be sterile due to a contaminant.

Moderate risk, FDA, , Sterility problem

Medline Neuro Sponges

Medline Neuro Sponges may have higher-than-expected endotoxin levels.

Moderate risk, FDA, , Quality testing problem

Medline Guidewires, Syringes and Kits

Medline Namic Guidewires, syringes, and kits have had regulatory clearances rescinded.

Moderate risk, FDA, , Device defect

Medline Convenience Kits with 10mL Polycarbonate Colored Syringes

Medline Convenience Kits with 10mL polycarbonate syringes have unapproved design changes.

Moderate risk, FDA, , Unapproved product

Medline CENTURION Circumcision Kit

The CENTURION Circumcision Kit was distributed without required sterilization and is not sterile.

Moderate risk, FDA, , Sterility problem

Medline Namic Angiographic Control Syringes and Medical Convenience Kits

NAMIC Angiographic Rotating Adaptor (RA) Control Syringes may unwind during use, causing a loose or full disconnection.

High risk, FDA, , Device defect

Medline Bronchoscopy and Airway Kits

Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves.

Moderate risk, FDA, , Foreign object

Medline Enfit g-Tube Connector

The ENFIT G-TUBE CONNECTOR may not seal properly, leading to leakage that could cause delayed care and fluid loss.

Moderate risk, FDA, , Device defect

Medline Sterile Radiology Procedure Kits

Sterile Radiology Procedure Kits may have a breach in sterile packaging, compromising sterility.

Moderate risk, FDA, , Sterility problem

Puracol and Puracol Plus Collagen Wound Dressings

Puracol and Puracol Plus Collagen Wound Dressings have elevated endotoxin levels that may cause strong inflammatory response.

Moderate risk, FDA, , Contamination

Medline Open Heart, Cardiac Procedure and Cardio Congenito Kits

The chest drainage units have updated instructions to clarify they are for adults only.

Moderate risk, FDA, , Device defect

Medline Medcrest Surgical Gowns and Surgical Drapes

Medline Medcrest Surgical Gowns may experience premature delamination, which can cause brief delays in patient care and risk of infection.

Moderate risk, FDA, , Device defect

Medline Kits with Tego Connectors

Medline kits containing Tego Connectors may have silicone seal issues that can cause fluid leakage or air infusion.

Moderate risk, FDA, , Contamination

Medline Sterile Saline Wound Wash and Convenience Kits

Medline Sterile Saline Wound Wash may not meet sterility requirements.

Moderate risk, FDA, , Sterility problem

Medline Convenience Kits and Surgical Drapes

Medline Convenience Kits and Surgical Drapes may not be sterile due to calibration issues in sterilization equipment.

Moderate risk, FDA, , Sterility problem

Medline IV Administration and Extension Sets

IV administration and extension sets may leak, crack, or break, causing treatment delays, blood loss, infection, air embolism, or underdosage.

Moderate risk, FDA, , Device defect

Medline Medical Convenience Kits

Medline medical convenience kits may have an open seal on the packaging of the applicators.

Moderate risk, FDA, , Device defect

Medline ReNewal Reprocessed Diagnostic Catheters

Reprocessed catheters may contain small particles of residual material.

High risk, FDA, , Foreign object

Medline Suction Catheter Kits and Intubation Tray

Medline Suction Catheter Kits and Intubation Tray may contain a smaller 8 Fr catheter, which can cause airway obstruction.

Moderate risk, FDA, , Device defect

Medline Medical Procedure Convenience Kits

Medline medical procedure convenience kits contain a liquid adhesive whose tubing can crack during actuation.

Moderate risk, FDA, , Device defect

Medline Semi Electric and Full Electric Homecare Beds

Medline beds have a potential hazard involving the hand control pendant and wires, which may overheat and pose a fire risk.

High risk, FDA, , Device defect

Medline Medical Procedure Convenience Kits

Medline medical procedure convenience kits can leak and emit vaporized saline that resembles smoke during use.

Moderate risk, FDA, , Device defect

Medline Kits With B. Braun IV Administration Sets

Medline kits containing B. Braun IV administration sets may have check valves that stick.

Moderate risk, FDA, , Device defect

Medline Hudson RCI Medium Concentration Oxygen Masks

Medline Hudson RCI Medium Concentration Oxygen Masks can have tubing disconnect, delaying patient care and causing shortness of breath.

Moderate risk, FDA, , Device defect
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