Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Container fill and transfer sets Recalled by The Metrix Company Due to An issue was identified after a redesign of...
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 The Metrix Company directly.
Affected Products
Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL.
Quantity: 137,598 cases
Why Was This Recalled?
An issue was identified after a redesign of the auto compounding device. The compounder cannot meet the designed accuracy specification when dispensing into bags. After reviewing the initial design of the device, it was determined the dispensing volume validation was not properly done and none of the compounders on the market can meet the stated specifications.
Where Was This Sold?
This product was distributed to 20 states: AL, AZ, CA, CO, CT, FL, IL, IA, KS, LA, MD, MA, MN, NC, OH, PA, TN, TX, UT, WA
About The Metrix Company
The Metrix Company has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report