Ohio recalls
4745 federal recalls on file affecting Ohio - 760 Ohio-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Robinson catheters recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Oral Restoration Kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline vasectomy reversal kit recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline cardiac procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline cardiac procedure kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline laparoscopy kits recalled for catheter defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline latex catheter recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline latex catheter recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheter trays recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheter tray recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheterization trays recalled for defects
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline urethral catheters recalled for connector detachment risk
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
- 2026-06-24FDA-DeviceMito Red LightClass IINationwideMito Red Light Super Mobile recalled for battery fire risk
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed recalled for loose fastener risk
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed Carestation recalled for fastener hazard
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed recalled for loose fastener risk
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert issue
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal surgical trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal access port recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceHowmedica OsteonicsClass IINationwideHowmedica Triathlon Baseplate Size 3 recalled for mislabeling
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
Get notified about new Ohio recalls
Free weekly digest. Add Ohio to your profile to filter alerts to your state.
Get the Sunday Brief