Check a product
Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline convenience kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline convenience kits recalled for cracked tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline LAVH kits recalled for defective adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline C-section kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline pelviscopy kit recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline delivery kit recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline neuro kits recalled for defective adhesive
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline hernia repair tote kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline dressing change kit recalled for defective tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline IV Start Kit recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for defective adhesive
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline convenience kits recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline convenience kits recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline catheter kits recalled for defective adhesive tubing
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline nerve block kits recalled for tubing crack risk
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline nerve block trays recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedline Industries, LPClass IIMedline EBSI Kit recalled for defective adhesive tubing
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.
- 2026-06-24FDA-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIPhilips Allura Xper recalled for hand switch button malfunction
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.
- 2026-06-24FDA-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIPhilips MultiDiagnost Eleva X-ray systems recalled for hand switch malfunction
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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International arterial catheter kits recalled for sterilization concerns
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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International CVC kits recalled for sterility and anesthetic concerns
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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International PICC Access Tray recalled for sterility risk
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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for contaminated anesthetic
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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for sterility concerns
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.