FDA Recall Completed

Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller

Recall: Z-1919-2025 · Initiated May 13, 2025

Recall

Recall Number
Z-1919-2025
Event Number
96849
Firm
Cardinal Health 200, LLC
FEI Number
3001236905
Product Code
JOW
Status
Completed
Root Cause
Software change control
Initiated
May 13, 2025
Posted
June 6, 2025
Address
3651 Birchwood Dr, Waukegan, IL, 60085-8337

Description

Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller

Reason

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Action

On May 13, 2025, the firm began to notify customers via Urgent Medical Device Product Correction letters. Customers were informed of the issue, which exclusively impacts use of the Comfort Small Knee Sleeve. Other sleeve sizes are unaffected and operate as intended with the SmartFlow Controller. The product remains operational if the Comfort Small Knee Sleeve and SmartFlow Controller configuration is not utilized during therapy. A software update on the SmartFlow Controller is necessary before using the SmartFlow controller with the Comfort Small Knee sleeve configuration. Customers should discontinue use of the Comfort Small Knee Sleeve with the SmartFlow Controller and utilize a suitable alternative such as SM thigh or foot cuff. Customer service representatives will coordinate with customers to facilitate a software update which will allow the controllers to be utilized with the small knee sleeves without causing the error.

Distribution

Domestic US distribution to AK, CA, FL, MA, TX. International distribution to Japan.

Quantity

6517 cases total