Wisconsin recalls

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.

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.

The hand switch button on certain Philips Allura Xper fluoroscopy systems may not fully release after use. This can result in loss of imaging capability, unintended radiation exposure, or unintended contrast injection during procedures.

The hand switch button on certain Philips MultiDiagnost Eleva X-ray imaging systems may not fully release after use. This malfunction could prevent the system from stopping imaging, potentially leading to unintended radiation exposure or extra contrast dye injection.

Arrow International recalled multiple arterial catheter kits because they contain lidocaine, bupivacaine, and saline solution from a supplier with quality control issues. If the sterilization of these injectable products was compromised, patients could face serious or life-threatening infections.

Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality issues in three models of central venous catheter (CVC) kits. The supplier's products showed limited reports of drug ineffectiveness, and compromised sterility in injectable products could cause serious injury.

Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with known quality issues in PICC Access Tray kits. The supplier's products have reported cases of drug ineffectiveness, and compromised sterility in injectable medications can cause serious injury. About 360 kits with specific lot numbers were distributed nationwide.

Arrow International catheter kits contain lidocaine, bupivacaine, and saline solution from a supplier with quality control issues. The supplier's products may not be sterile or effective. If these injectable components are contaminated, they could cause serious or life-threatening infections.

Arrow International recalled multiple PSI and MAC catheter kits because they contain lidocaine, bupivacaine, and saline from a supplier with quality issues. The supplier's products may not be sterile, and there have been limited reports that the medications did not work as expected. If the sterility of these injectable products is compromised, patients could experience serious or life-threatening infections.

Arrow International's ACCESS TRAY kits (model ASK-04001-MC3) contain injectable anesthetic and saline solutions from a supplier with documented quality issues. If the sterility of these water-based injectables has been compromised, serious or life-threatening infections could result. The supplier also reported limited cases of drug ineffectiveness.

Arrow International included lidocaine, bupivacaine, and saline solutions from a supplier with documented quality problems in multiple arterial catheter kits and sets. The supplier's medications showed signs of ineffectiveness, and if sterility was compromised, the kits could cause serious injury when used.

Arrow International included lidocaine, bupivacaine, and saline solutions from a supplier with quality issues in three central access kits. The supplier's quality problems and limited reports of drug ineffectiveness raise concerns that sterility may be compromised, which could lead to serious infection or other life-threatening complications.

Arrow International included injectable medications (lidocaine, bupivacaine, and sodium chloride) from a supplier with quality issues in multiple spinal anesthesia kits. The supplier's products may not be sterile or effective, which could cause serious injury during spinal procedures.

Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality issues in multiple hemodialysis and AHDC kits. The supplier's products have been linked to drug ineffectiveness and potential sterility failures. Compromised sterility in injectable products can cause serious or life-threatening infections.

Arrow International included anesthetic and saline solutions from a supplier with documented quality issues in PI Midline midline catheter kits. The supplier's products showed signs of ineffectiveness and potential sterility problems, which could compromise the safety of these injectable medical devices.

Arrow International included anesthetic drugs (lidocaine and bupivacaine) and saline solution from a supplier with quality problems into paracentesis kits. The supplier had reports of drug ineffectiveness, and if the sterility of these injectable products was compromised, patients could face serious injury.