Medline

Medline found that samples of its 15 Fr urethral catheterization trays did not meet quality standards. Problems included rough spots on the catheter surface, connectors that could detach from the catheter funnel, and catheters with incorrect outer diameter in some cases.

Medline Industries recalled its Pre-connected Urethral Catheterization Tray (15 Fr, model DYND10407) after finding that some units did not meet quality standards. Problems included rough catheter surfaces, premature separation of the connector from the funnel, and variations in catheter diameter. No injuries have been reported.

Medline identified that some urethral catheterization trays (15 Fr size, product numbers DYNC1816 and DYND10350) did not meet quality standards. Problems include irregular catheter surface finish, connectors that may detach prematurely from the catheter funnel, and some catheters with incorrect outer diameter.

Medline identified that samples of their red rubber latex urethral catheters did not meet performance standards. Issues included rough surface finishes, connectors that detached prematurely from the catheter funnel, and some catheters with outer diameters outside specification. This recall affects 11 product sizes distributed worldwide.

Medline convenience hysterectomy kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in these kits may crack when used, making the adhesive unusable for application.

Medline convenience kits used in C-section procedures contain a recalled adhesive product with defective tubing that may crack during use, making the adhesive unusable. The affected kits were distributed nationwide. No injuries have been reported.

Medline convenience kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive with defective tubing. The butyrate tubing in these kits may crack when used, making the adhesive unusable for medical application.

Multiple Medline surgical convenience kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive where the tubing may crack during use, making the adhesive unusable. This affects kits used in cardiac, vascular, and pacemaker procedures.

Medline convenience kits for port-a-cath procedures contain a recalled batch of MASTISOL Liquid Adhesive from Ferndale Laboratories. The tubing in these kits may crack during use, making the product unusable.

Medline femoral block tray kits (model DYNJRA1739B) contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The tubing in these adhesive applicators may crack when used, making the product unusable for its intended application.

Medline surgical convenience kits contain a recalled lot of Mastisol Liquid Adhesive from Ferndale Laboratories. The adhesive's butyrate tubing can crack during use, making the product unusable in surgical settings. No injuries have been reported.

Medline convenience kits (Driveline Management Kit EBSI1688 and Port Dressing Change Kit EBSI1328A) contain a recalled adhesive product with defective tubing. The tubing may crack when used, making the adhesive unusable. About 49,600 kits have been distributed nationwide.

Medline convenience kits containing central venous catheter (CVC) insertion supplies include a recalled lot of adhesive that can cause the tubing to crack when used. This may render the kit unusable for the intended medical procedure. No injuries have been reported.

Several Medline convenience kits used for central line, PICC, dialysis, and port access dressing changes contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The tubing in these adhesive bottles may crack when used, making the product unusable.

Medline Industries' Centurion convenience kits—used for central line, dialysis, and port dressing changes—contain a recalled batch of Mastisol Liquid Adhesive with defective tubing. The tubing may crack when squeezed, making the adhesive unusable for patient care.

Medline Industries is recalling over 49,000 surgical convenience kits that contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The tubing in the adhesive applicator may crack during use, making the product unusable in the operating room.

Medline convenience kits (Basic Eye and Tubal Ligation models) contain a recalled adhesive product from Ferndale Laboratories. The tubing in the adhesive applicator may crack when used, making the kit unusable.

Medline convenience kits (model DYNJ908031D) contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in these adhesive bottles may crack when used, making the product unusable. No injuries have been reported.

Medline convenience kits contain a recalled lot of MASTISOL Liquid Adhesive from Ferndale Laboratories. The butyrate tubing in these kits may crack during use, making the adhesive unusable.

Medline convenience kits contain a recalled lot of MASTISOL Liquid Adhesive from Ferndale Laboratories. The tubing in the adhesive may crack when used, making the product unusable.

Medline convenience kits used in robotic and laparoscopic surgery contain a recalled lot of adhesive from Ferndale Laboratories. The tubing in the adhesive applicator may crack during use, making the product unable to be applied properly during surgery.

Medline's SMSC-PELVISCOPY convenience kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The tubing in these kits may crack when used, making the adhesive unusable for its intended application.

Medline convenience kits used in labor and delivery and C-section procedures contain a recalled lot of MASTISOL Liquid Adhesive from Ferndale Laboratories. The tubing in these adhesive bottles may crack when used, making the product unable to be applied properly.

Medline Industries recalled multiple neurosurgery convenience kits because they contain a defective lot of MASTISOL Liquid Adhesive from Ferndale Laboratories. The tubing in the adhesive applicator may crack when used, making the product unusable for the procedure.

Medline convenience kits for hernia repair contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in these kits may crack when used, making the adhesive unusable for its intended application.

Medline's pediatric dressing change convenience kit contains a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive with a manufacturing defect. The tubing may crack when you try to use it, making the adhesive unusable.

Medline's IV Start Kit with HubGuard (model DYNDV2662) contains a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in these kits may crack when used, making the kit unusable for its intended purpose.

Medline convenience kits containing a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive are being recalled. The adhesive's butyrate tubing can crack during use, making the adhesive unusable in surgical settings. About 50,000 kits across multiple surgical types are affected.

Medline's plastic surgery convenience kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive with a manufacturing defect. The adhesive's butyrate tubing may crack when used, making the product unable to function properly during surgery.

Medline Industries distributed multiple surgical convenience kits containing a recalled lot of Mastisol Liquid Adhesive from Ferndale Laboratories. The adhesive tubing may crack when used, making the product unusable during procedures.