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# Metrix Recalls IV Flexible Bags
- URL: https://www.fdaweb.com/metrix-recalls-iv-flexible-bags/
- Published: 2019-09-10T12:00:00.000Z
- Updated: 2026-09-15T01:48:56.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144972

The Metrix Co. (Dubuque, IA) has recalled several lots of its empty IV flexible containers (bag) marketed under the Metrix Secure EVA Dual Chamber and Baxter ExactaMix names, due to the potential for leakages from the IV bag at the chamber divider rod, which could result in a serious infection to patients. The bags are used in an intravenous admixture program, and to store and deliver intravenous parenteral admixtures to patients. The empty bag is filled with parental admixtures by a healthcare provider (e.g. licensed pharmacist) under normal pharmacy conditions, e.g. laminar flow hood.

The recall was initiated after the company received eight complaints of leaking bags, according to a [recall notice](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/metrix-company-dubuque-iowa-recalling-specific-lots-empty-iv-flexible-containers-bag-marketed-under?ref=fdaweb.com). It says an “investigation indicates the problem was caused by the assembly machine malfunction, creating additional stress on the rod, channel and bag film resulting in a potential to cause a material anomaly that is concealed until the rod is removed at the point of use.”