Kansas recalls
3721 federal recalls on file affecting Kansas - 343 Kansas-specific plus 3378 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-04FDA-DeviceAgiliti HealthClass IINationwideCheck your Agiliti Adapt Pump settings
Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management function after using the Autofirm function for 10 minutes. This issue only occurs when the 10-minute timer is allowed to elapse after the Autofirm button is pressed after initial setup, and it only affects the Microclimate Management function.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline dialysis dressing change kits
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using recalled dialysis dressing kits
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceMedlineClass IINationwideMedline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using affected Medline dialysis kits
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline dialysis on/off kits (SKU EBSI1746)
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using affected Medline dialysis kits
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
- 2026-03-04FDA-DeviceEdermyClass IINationwideStop using Edermy PIE PAK devices
Lack of 510K clearance
- 2026-03-04FDA-DeviceEdermyClass IINationwideStop using Edermy PIE Trolley System Model 2005
Lack of 510K clearance
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck your Encore Medical shoulder implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck Encore Medical knee implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceEncore MedicalClass IINationwideCheck reverse shoulder implant labeling
Knee and Humeral socket implants contain incorrect labeling.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A2666T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2642
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2641
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Model A37004A sheaths
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideContact Olympus about recalled urological sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus resection sheath Model A2666
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus WA22017T inner sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath WA22017A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A4741
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A42011A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2660
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A22043T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath 28 Fr.
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A22042T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A22042A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A22041T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath 24 Fr
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Inner Sheath A22040T
Complaints of the ceramic tip of the resection sheath breaking have been received.
Get notified about new Kansas recalls
Free weekly digest. Add Kansas to your profile to filter alerts to your state.
Get the Sunday Brief