Medline recalls

Medline is recalling 34 convenience and procedure kits because they contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack during use, making the product unusable for application. No injuries have been reported.

Moderate·FDA·Jun 24, 202634 products

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.

Moderate·FDA·Jun 3, 2026

Medline is recalling seven procedure kit products that contain bupivacaine hydrochloride in dextrose injection made by Huons Co. That bupivacaine was itself recalled over quality problems, including questions about microbiology testing data and reports of reduced effectiveness. No injuries have been reported.

Serious·FDA·Jun 3, 20267 products

Medline recalled 11 products, including Namic angiographic and Preceptor manifolds and medical convenience kits that contain Namic manifolds. Medline found particulate matter in the fluid path of the manifolds. No injuries have been reported, and the products were distributed in the US and several other countries.

Serious·FDA·May 20, 202611 products

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.

Moderate·FDA·Apr 22, 2026

Medline is recalling 19 NAMIC angiographic syringes and Medline convenience kits that contain them. The syringe's rotating adaptor can unwind during use, which may loosen or fully disconnect the syringe from the manifold. No injuries have been reported.

Serious·FDA·Apr 15, 202619 products

Medline is recalling 7 kit products that contain Olympus single-use biopsy valves, totaling about 14,379 kits. Olympus found more complaints of rubber fragments detaching from a slit in the valves. A loose fragment could lodge in a patient's airway and may need to be removed in a procedure. No injuries have been reported.

Serious·FDA·Apr 8, 20267 products

Medline Industries identified a potential breach in the sterile pouch packaging of one lot of Sterile Radiology Procedure Kits (Model DYNDH1491B). This breach may allow the kit to lose its sterile condition. No injuries have been reported.

Moderate·FDA·Apr 8, 2026

Medline recalled two products: ENFit G-tube connectors and kits that contain them. The connectors were not made to required dimensions, so they may not seal properly with ENFit-style devices and can leak. No injuries have been reported.

Moderate·FDA·Apr 8, 20262 products

Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.

Serious·FDA·Apr 1, 2026

Medline is recalling 2 product groups of surgical gowns and drapes, about 127,572 units in total. The fabric may separate in layers (delaminate) early when washed using the included laundering instructions. If a separated product is used during surgery and fluid passes through, there may be a risk of infection.

Moderate·FDA·Mar 18, 20262 products

Medline and Cardinal Health have recalled specific lots of chest drainage kits used in cardiac surgery because the instructions needed to clarify that these devices are intended only for adult patients age 18 and older. The kits were distributed nationwide in California and internationally to Chile and Panama.

Moderate·FDA·Mar 18, 2026

Medline is recalling six kits that include Tego Connectors, including dialysis, central line, and dressing change kits from Medline and Centurion. Affected lots may have silicone seal doming or tearing, which can block fluid flow, delay or interrupt therapy, cause leakage, or allow air or biological contaminants into the body. No injuries have been reported.

Moderate·FDA·Mar 4, 20266 products

Medline reported that the manufacturer of its sterile saline wound wash may not have made the products to the required sterility assurance level. The recall covers five products: a saline wound wash sold under the Medline and Meijer names, plus several Medline convenience kits. No injuries have been reported, and the products were distributed across the US and to the Bahamas, Bermuda, and the Cayman Islands.

Moderate·FDA·Mar 4, 20265 products

Medline is recalling 42 convenience kits and procedure packs that were sterilized and packaged on equipment with calibration problems. The kits went through the validated sterilization and packaging cycles, but the calibration issues could affect how reliably they are sterile. No injuries have been reported.

Moderate·FDA·Feb 25, 202642 products

Medline Industries is recalling 23 models of IV administration and extension sets because the male connectors may leak, crack, or break during use under certain conditions. This could cause delays in treatment, blood loss, infection, air embolism, or patients not receiving the correct medication dose.

Serious·FDA·Feb 25, 2026

Medline is recalling 11 kit products that contain BD ChloraPrep Triple Swabsticks. BD found that the applicator packaging may have an open seal. No injuries have been reported.

Moderate·FDA·Feb 18, 202611 products

Medline is recalling seven groups of reprocessed heart and ultrasound catheters because they may contain small particles of leftover material. If these devices are used, the particles could cause inflammation, infection, or blood clots, which may lead to embolism or deep vein thrombosis. This is an expansion of an earlier recall, and the affected catheters were distributed nationwide.

Serious·FDA·Feb 18, 20267 products

Medline is recalling two suction catheter kit products, with about 142,100 units affected. Some kits may contain an 8 Fr suction catheter instead of the required 14 Fr catheter. Using the smaller catheter could partly or fully block the airway and reduce oxygen. No injuries have been reported.

Serious·FDA·Feb 18, 20262 products

Medline recalled 15 medical procedure convenience kits that contain MASTISOL liquid adhesive. Complaints reported that the butyrate tubing cracked when the adhesive vials were activated. No injuries have been reported.

Moderate·FDA·Feb 4, 202615 products

Medline is recalling six models of electric homecare beds, about 599,000 units in total. In rare cases, such as overloading the bed, an obstruction blocking its movement, or a jammed motor, the hand control pendant and its cords can overheat and, in rare instances, catch fire. Medline has received 58 complaints of pendants sparking, burning, melting, smoking, or catching fire. No injuries have been reported.

Serious·FDA·Jan 28, 20266 products

Medline is recalling six groups of surgical convenience kits, about 59,000 units in total, that include Stryker Strykeflow 2 Suction Irrigators. A 2024 design change lets irrigation solution reach the handpiece and battery pack, which can cause the device to leak or give off vaporized saline that may look like smoke. No injuries have been reported.

Moderate·FDA·Jan 21, 20266 products

Medline is recalling 12 kits that contain B. Braun IV administration sets and pump administration sets. Customers reported that the check valve components in these sets can get stuck in the open or closed position. No injuries have been reported.

Moderate·FDA·Jan 21, 202612 products

Medline Industries is recalling multiple models of Hudson RCI oxygen masks because the tubing can disconnect during use. If this happens, oxygen delivery stops, which can delay patient care and cause breathing problems that may require medical intervention.

Serious·FDA·Jan 14, 2026

Medline is recalling 2 sterile surgical products, sold nationwide and distributed in CA, CO, IL, KS, and MI, because their packaging seals may be weak. If a seal fails, sterility may be lost, which could raise the risk of infection if the product is used. No injuries have been reported.

Moderate·FDA·Dec 24, 20252 products

Medline Industries is recalling DEXLOCK Achilles Repair Implant Kits (model MAKT4520, lot 19019) because the drill bit can fuse to the drill guide during surgery. This can delay the procedure while a replacement drill bit and guide are retrieved. No patient injuries have been reported.

Moderate·FDA·Dec 17, 2025

Medline is recalling seven Curad bandage products, including Germ-Shield Touch-Free, Quick Strip, and Fur Friends fabric and plastic bandages. Some packages may have open seals, which could compromise the sterility of the bandages. No injuries have been reported.

Moderate·FDA·Dec 17, 20257 products

Medline is recalling specific batches of Medline Perfusion Syringes (model DYNJ39223C) that contain BD Luer Tip Caps. BD's testing found that certain tip cap trays failed biocompatibility tests, meaning the plastic may cause skin irritation, allergic reactions, or other adverse effects if it contacts patients during use. No injuries have been reported so far.

Moderate·FDA·Dec 17, 2025

Medline is recalling 20 kit products that contain SafeAir Smoke Evacuation Pencils made by Stryker Instruments. The recall was expanded to add 47 more pencil lots to an October 2024 recall, because the pencils may activate without manual input when plugged into a power source, or stay active after the buttons are released. No injuries have been reported.

Moderate·FDA·Nov 26, 202520 products

Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.

FDA·Nov 26, 2025