Ohio recalls
3777 federal recalls on file affecting Ohio - 702 Ohio-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-04FDA-DevicePhilipsClass IINationwideContact Philips about your Ingenia 3.0T CX MRI system
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- 2026-02-04FDA-DevicePhilipsClass IINationwideContact Philips about your Ingenia 3.0T MRI system
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- 2026-02-04FDA-DevicePhilipsClass IINationwideContact Philips about your Ingenia 1.5T MRI system
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- 2026-02-04FDA-DevicePhilipsClass IINationwideContact Philips about Evolution Upgrade 3.0T MR system
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- 2026-02-04FDA-DevicePhilipsClass IINationwideCheck Philips MRI elastography software
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- 2026-02-04FDA-DeviceCardinal HealthClass IINationwideStop using Cardinal Health chest drainage units on infants
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older. When used on infants, the CDU may not demonstrate tidaling/bubbling, which may confound the clinician's assessment of device functionality and lead to inadequate/inappropriate treatment/therapy, delay to treatment/therapy, and prolonged hospitalization.
- 2026-02-04FDA-DeviceZimmer BiometClass IINationwideCheck your Zimmer A.T.S. 3200TS tourniquet software
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
- 2026-02-04FDA-DeviceZimmer BiometClass IINationwideCheck your Zimmer tourniquet system software
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
- 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
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