Oregon recalls
4500 federal recalls on file affecting Oregon - 492 Oregon-specific plus 4008 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Centurion kits recalled for tubing crack risk
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for cracked tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline LAVH kits recalled for defective adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline C-section kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline pelviscopy kit recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline delivery kit recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline neuro kits recalled for defective adhesive
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline hernia repair tote kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline dressing change kit recalled for defective tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline IV Start Kit recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for defective adhesive
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline catheter kits recalled for defective adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline nerve block kits recalled for tubing crack risk
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline nerve block trays recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline EBSI Kit recalled for defective adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DevicePhilipsClass IINationwidePhilips Allura Xper recalled for hand switch button malfunction
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
- 2026-06-24FDA-DevicePhilipsClass IINationwidePhilips MultiDiagnost Eleva X-ray systems recalled for hand switch malfunction
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
- 2026-06-24FDA-DeviceArrowClass INationwideArrow International arterial catheter kits recalled for sterilization concerns
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
- 2026-06-24FDA-DeviceArrowClass INationwideArrow International CVC kits recalled for sterility and anesthetic concerns
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
- 2026-06-24FDA-DeviceArrowClass INationwideArrow International PICC Access Tray recalled for sterility risk
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
- 2026-06-24FDA-DeviceArrowClass INationwideArrow International catheter kits recalled for contaminated anesthetic
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
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