Iowa recalls
3,476 federal recalls affecting Iowa in the last 12 months - 123 Iowa-specific plus 3,353 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline arterial insertion and PICC dressing kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for defective adhesive tubing
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline port-a-cath kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline femoral block tray kits recalled for tubing defect
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline medical kits recalled for cracked adhesive tubing
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline CVC insertion kits recalled for tubing failure
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline dressing change kits recalled for adhesive tubing defect
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Centurion kits recalled for tubing crack risk
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.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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-DeviceMedlineClass IINationwideMedline 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.
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