The Metrix Company SECURE 250 mL EMPTY EVA CONTAINER With 2 Ports, REF 66045 recall — FDA Z-0339-2025
A limited number of IV bags have been found to leak during filling.
Overview of recall records associated with The Metrix Company, including dates, categories and classifications where available.
Classification mix: Class II: 24.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
A limited number of IV bags have been found to leak during filling.
Potential for leaking product
Potential for leaking product
Potential for leaking product
Potential for leaking product
Potential for leaking product
Potential for leaking product
Potential for leaking product
Potential for leaking product
This page summarizes recall records in which the official source identifies The Metrix Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.