Oregon recalls
3844 federal recalls on file affecting Oregon - 465 Oregon-specific plus 3379 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline surgical kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline C-section kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using Medline circumcision procedure kit
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using Medline surgical procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline neuro procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideCheck Medline procedure kits for cracked adhesive applicators
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using Medline HEAD SHAVE-LATEX SAFE KIT
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using recalled Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideCheck your Medline surgical kit lot numbers
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using affected Medline procedure kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceMedlineClass IINationwideStop using Medline Nerve Block Tray 2 kits
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- 2026-02-04FDA-DeviceNiproClass IINationwideStop using NIPRO Conductivity Standard Solution
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using Gold Star Distribution pregnancy tests
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled Oral-B and Colgate toothbrushes
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled feminine hygiene products
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled Trojan condoms
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using Gold Star first aid kits and bandages
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideContact Canon Medical about your Alphenix X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS Q.namix T system
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
- 2026-02-04FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS Q.namix R X-ray system
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm AlternatiV+ anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm AlternatiV+ Max anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm suture anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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