Medline

Medline Industries issued a recall of nearly 50,000 surgical convenience kits because they contain a defective lot of Mastisol Liquid Adhesive made by Ferndale Laboratories. The tubing on the adhesive dispenser may crack when used, making the product unusable during surgery.

Medline convenience kits containing a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive have been distributed nationwide. The butyrate tubing in these kits may crack when the adhesive is dispensed, making the product unusable.

Medline convenience kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive with defective tubing. The butyrate tubing may crack when the applicator is used, making the adhesive unusable for wound dressing or catheter applications.

Multiple Medline surgical convenience kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive with defective tubing. The butyrate tubing may crack when used, making the adhesive unusable during surgical procedures.

Medline Industries' Minor Cath Lab Pack, Vascular Angio Pack, and Port-a-Cath kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack when used, making the kits unusable for their intended medical application.

Medline Industries nerve block kits contain a recalled adhesive component from Ferndale Laboratories. The tubing in these kits may crack when used, making the product unable to function properly for patient care.

Medline nerve block kits contain a recalled adhesive component from Ferndale Laboratories that may cause the tubing to crack when used. If the tubing cracks, the kit cannot be used as intended for the procedure.

Medline EBSI Kits (model EBSI1534) contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The tubing in these kits may crack during use, making the product unusable. No injuries have been reported.

Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.

Medline distributed multiple spinal anesthesia and nerve block procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection made by Huons Co. The anesthetic was recalled due to quality concerns, including problems with microbiology testing data and reports that the medication may not work as expected.

Medline has identified particulate (small particles) in the fluid path of Namic Manifolds within certain TAVI medical convenience kits. The kits were distributed nationwide and internationally. No injuries have been reported.

Medline has identified particles inside the fluid pathways of Namic Manifolds used in cardiac catheterization kits. These kits are used during heart procedures. The contamination could potentially affect the performance of the devices during medical procedures.

Medline has identified particles in the fluid pathway of certain cardiac catheterization manifold kits used in heart procedures. The affected kits span multiple product lines and lot numbers manufactured between 2024 and 2025. No injuries have been reported.

Medline identified particles inside the fluid pathways of Namic Manifolds used in three medical convenience kits: Angiography Cath Lab, Cath Lab Pack, and Angio Kit. These particles could potentially affect the performance of the manifold during use. Approximately 508 kits have been distributed across the U.S. and several other countries.

Medline has identified particulate matter inside the fluid pathway of certain Namic Preceptor Manifold blood pressure transducers. This contamination could affect the accuracy of blood pressure readings or damage the device during use. No injuries have been reported to date.

Medline has identified particles inside the fluid path of certain Namic Preceptor Manifold blood pressure transducers. These particles could interfere with accurate blood pressure readings or damage the device during use.

Medline identified small particles present inside the fluid pathways of certain Namic Angiographic Manifolds used in cardiac bypass procedures. These manifolds are medical devices that control and direct fluid flow during heart surgery. The contamination was discovered in 1,975 units across multiple lot numbers.

Medline has identified particles in the fluid pathway of certain Namic Angiographic Manifolds used in cardiopulmonary bypass procedures. These manifolds are used to manage fluid flow during heart and lung bypass surgery. The contamination could potentially affect the safety and performance of the device during use.

Medline Industries identified particulate matter in the fluid path of certain Namic Angiographic Manifolds used in cardiopulmonary bypass procedures. The contamination could potentially affect the safety and performance of these critical medical devices during use.

Medline distributed one lot of CENTURION Circumcision Kits (lot number 25KLA002) without completing the required sterilization process. This means the kits are not sterile and could pose an infection risk if used. The affected kits were distributed in South Carolina.

Medline has recalled certain shoulder arthroscopy and extremity medical convenience kits because the syringe adapter may unwind during use. This could cause the syringe to loosen or disconnect from the manifold, potentially disrupting a medical procedure. No injuries have been reported.

Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes may have a defect where the syringe adapter can unwind during use. This could cause the syringe to loosen or fully disconnect from the manifold during a procedure, potentially affecting patient care.

Medline has recalled specific batches of medical convenience kits used in robotic procedures because the syringe rotating adaptor may unwind during use. This can cause the syringe to loosen or fully disconnect from the manifold, potentially affecting the procedure. No injuries have been reported.

Medline Industries has recalled certain medical convenience kits containing NAMIC angiographic syringes because the syringe adapter may unwind during use. This could cause the syringe to loosen or disconnect from the manifold, potentially compromising the procedure.

Medline has recalled certain medical convenience kits used in angiography and neurointerventional radiology procedures. The syringe rotating adapter in these kits can unwind during use, potentially causing a loose connection or complete disconnection between the syringe and manifold. This could interrupt fluid delivery during medical procedures.

Medline Industries identified a defect in NAMIC Angiographic Rotating Adaptor syringes included in certain medical convenience kits. The syringe adaptor may unwind during use, causing the syringe to loosen or separate from the manifold. This could affect the delivery of contrast media or other fluids during medical procedures.

Medline Industries has recalled multiple medical convenience kits that contain NAMIC Angiographic Rotating Adaptor syringes. The syringe's rotating adapter may unwind during use, causing the connection between the syringe and manifold to loosen or fully disconnect. This could interrupt fluid flow or medication delivery during procedures.

Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes may have a defective rotating adaptor that can unwind during use. This could cause the syringe to disconnect from the manifold during a medical procedure. The issue affects 60 kits distributed in the US and 10 other countries.

Medline has recalled three medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes used in surgical procedures. The syringe adapter may unwind during use, causing the syringe to disconnect from the manifold and potentially disrupting the procedure.

Medline has recalled certain medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes used in cardiac catheterization and other procedures. The syringe adaptor may unwind during use, causing a loose or complete disconnection between the syringe and manifold, which could disrupt patient care.