The Metrix Company recalls empty EVA dual chamber containers (model H938901) used in IV admixture programs due to potential leaking. Affected units include specific lot numbers for 500ml and 2500ml sizes.
Potential for leaking product
The Metrix Company is recalling empty EVA dual chamber containers (model H938901) used for intravenous admixture storage because they may leak. This could cause contamination of medical solutions if the container leaks during use in a pharmacy setting.
These empty containers are designed to hold intravenous medications but may leak if not properly sealed. Leaks could contaminate the medication being prepared, potentially causing infections or incorrect dosing if the container is not used correctly.
Pharmacies and healthcare facilities that use these containers for intravenous medication preparation are most at risk. Patients are not directly affected as the containers are empty and only filled in pharmacy settings.
Check for the model number H938901 on the container. The product is an empty EVA dual chamber container with screw connectors, available in 500ml and 2500ml sizes. Affected units have specific lot numbers listed in the recall notice.
Inspect the container for signs of leakage or damage before use in pharmacy settings.
The containers are designed to be used in pharmacy settings but may leak if not properly sealed. They should be checked for leaks before use.
Check for the model number H938901 and specific lot numbers listed in the recall notice, which include 500ml and 2500ml sizes.
Inspect the container for leaks and ensure it is properly sealed before use in pharmacy settings. If leaks are found, contact your pharmacy for further guidance.
We’ve drafted a message you can send The Metrix Company to request your refund or repair — edit it as you like.
Subject: Recall Z-0007-2020 — The Metrix Company The Metrix Company Hello, I own a The Metrix Company that is covered by recall Z-0007-2020 from The Metrix Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
