Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medstream 81" (206 cm) 20 drop Universal Administration Sets. Disposable Recalled by US Infusion Inc dba Trucare Biomedix-USA Due to Several complaints regarding the IV sets leaking at...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact US Infusion Inc dba Trucare Biomedix-USA directly.
Affected Products
Medstream 81" (206 cm) 20 drop Universal Administration Sets. Disposable IV infusion set with 3 year expiration date.
Quantity: 62,700 IV sets
Why Was This Recalled?
Several complaints regarding the IV sets leaking at the Y site.
Where Was This Sold?
This product was distributed to 6 states: CA, GA, IL, MA, OH, TX
About US Infusion Inc dba Trucare Biomedix-USA
US Infusion Inc dba Trucare Biomedix-USA has 1 total recall tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report