Medline

Medline Industries is recalling certain lots of reprocessed ViewFlex Xtra ICE Catheters (9F x 90cm) because they may contain small particles of leftover material inside the device. If used, these particles could trigger inflammation, infection, blood clots, or other serious complications.

Certain lots of reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters distributed by Medline may contain small particles of leftover material from reprocessing. If used in patients, these particles could cause blood clots, infection, or inflammatory reactions that may lead to serious complications including stroke or blood clots in the lungs or legs.

Medline Industries is recalling certain lots of reprocessed Livewire Steerable Electrophysiology Catheters because they may contain small particles of residual material left after reprocessing. If used, these particles could cause serious complications including infection, blood clots, or emboli.

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Medline Industries is recalling certain reprocessed Webster CS Catheters because they may contain small particles of leftover material from cleaning. If used, these particles could trigger inflammation, infection, blood clots, or serious complications like stroke or lung clots.

Medline Industries intubation kits (SKU DYNJAA245B, lots 25IBC172 and 25HBJ413) may contain an 8 Fr suction catheter instead of the correct 14 Fr size. The smaller catheter can block the airway during intubation, potentially causing severe breathing problems or failure that requires emergency intervention.

Some Medline 14 Fr Suction Catheter Kits (SKU DYND40972) may contain a smaller 8 Fr catheter instead of the correct 14 Fr size. Using the wrong size catheter can partially or completely block the airway, leading to low oxygen levels and breathing failure that may require emergency treatment.

Medline medical procedure convenience kits containing MASTISOL liquid adhesive were recalled because the tubing can crack when the adhesive vial is opened. This could prevent proper use of the adhesive during surgery. No injuries have been reported.

Medline distributed three types of medical procedure kits containing MASTISOL liquid adhesive where the tubing can crack when the vial is opened. This could prevent proper adhesive application during cesarean section procedures. No injuries have been reported.

Medline distributed circumcision procedure kits (SKU DYNJ16826O) that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing on the adhesive vials can crack when opened, which could affect the sterility and usability of the adhesive during the procedure.

Medline distributed medical procedure convenience kits containing MASTISOL liquid adhesive with a manufacturing defect. The adhesive vials have butyrate tubing that can crack when opened, potentially compromising the adhesive's sterility and usability during procedures.

Medline distributed six types of neurosurgery procedure convenience kits containing MASTISOL liquid adhesive. The tubing in the adhesive vials can crack when opened, which may compromise the sterility or usability of the kit. No injuries have been reported.

Medline medical procedure convenience kits containing MASTISOL liquid adhesive were distributed with a manufacturing defect. The butyrate tubing in the adhesive applicator vials can crack when used, potentially affecting the adhesive's delivery or safety during medical procedures.

Medline medical procedure convenience kits (SKU P903933B) contain MASTISOL liquid adhesive with defective tubing that can crack when the vial is used. The cracked tubing could prevent proper product delivery during medical procedures.

Medline distributed 66 different medical procedure kits containing MASTISOL liquid adhesive with defective butyrate tubing that can crack when the vial is opened. The adhesive is used to secure medical devices during surgical procedures. No injuries have been reported.

Medline distributed eight types of medical procedure convenience kits that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing in the adhesive vials can crack when opened, which could affect the sterility or usability of the kit during medical procedures.

Medline distributed 30 types of surgical procedure convenience kits that contained MASTISOL liquid adhesive with a manufacturing defect. The tubing on the adhesive vials can crack when opened, potentially affecting the sterility of the kit. About 456 affected kits were distributed; no injuries have been reported.

Medline distributed nine types of medical procedure convenience kits containing MASTISOL liquid adhesive. The adhesive vials have defective tubing that can crack when used, potentially compromising the sterility and function of the kits. About 40 units were affected.

Medline distributed three medical procedure convenience kits containing MASTISOL liquid adhesive with a defect: the tubing can crack when the adhesive vial is opened. This affects breast-hernia-port, breast biopsy, and dermatology procedure kits. No injuries have been reported.

Medline distributed eight types of medical procedure convenience kits containing MASTISOL liquid adhesive. The adhesive vials had cracked butyrate tubing that could break when the vial is opened, potentially affecting the sterility or usability of the kit.

Medline medical procedure kits containing MASTISOL liquid adhesive were distributed with a defect: the tubing inside the adhesive vials can crack when opened. This affects two kit types used in cardiac catheterization and loop recovery procedures. No injuries have been reported.

Medline's Nerve Block Tray 2 kits contain MASTISOL liquid adhesive vials with tubing that can crack when opened. The cracked tubing could cause the adhesive to leak or not function as intended during medical procedures.

Medline Industries has recalled certain Full Electric Low Lightweight Homecare Beds (model MDR107003LO) because the hand control pendant and its wires can overheat and catch fire in rare situations—such as when the bed is overloaded, blocked, or has jammed parts. The company has received 58 reports of the pendant sparking, burning, melting, smoking, or catching fire.

The hand control pendant on Medline Full Electric Lightweight Homecare Beds (model MDR107003L) can overheat and catch fire in rare cases, especially if the bed is overloaded, blocked, or has jammed parts. Medline has received 58 reports of the pendant sparking, burning, melting, or smoking.

Medline's Full Electric Low Basic Homecare Bed (model MDR107003ELO) has a hand control pendant that may overheat and catch fire in rare cases—such as when the bed is overloaded, blocked from moving, or has jammed parts. Medline has received 58 reports of the pendant sparking, burning, melting, smoking, or catching fire. No injuries have been reported.

Medline Industries is recalling certain Full Electric Basic Homecare Beds because the hand control pendant and cord may overheat and catch fire in rare situations—such as when the bed is overloaded, blocked, or has jammed parts. The company has received 58 reports of the pendant sparking, burning, melting, or smoking.

Medline's Semi Electric Lightweight Homecare Bed (model MDR107002L) has a potential fire hazard in the hand control pendant and wires. In rare cases—such as when the bed is overloaded, blocked, or jammed—the pendant may overheat and spark, burn, melt, or catch fire. Medline has received 58 complaints of pendant sparking, burning, melting, smoking, or fire.

Medline's semi-electric homecare beds have hand control pendants that may overheat and catch fire in rare cases—for example, if the bed is overloaded, blocked, or jammed. The company has received 58 reports of the pendant sparking, burning, melting, or smoking.

Medline medical procedure kits containing Stryker's Strykeflow 2 Suction Irrigators may leak irrigation fluid into the handpiece and battery pack during use due to a 2024 design change. Some devices have leaked fluid or released vaporized saline that may resemble smoke.

Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.