Metrix recalls empty EVA dual chamber containers (H938905) used in IV admixture programs due to potential leaking. Affected units include specific lot numbers for 250ml/1250ml sizes. Contact Metrix for details.
Potential for leaking product
Metrix is recalling empty EVA dual chamber containers (model H938905) used for intravenous admixture storage because they may leak. This could cause medication spills or contamination if the containers are not properly sealed during use in pharmacies.
These empty containers are designed to hold medication in pharmacy settings but may leak if not properly sealed. Leaks could lead to medication spills or contamination during intravenous admixture preparation, potentially affecting patient safety.
Pharmacies and healthcare facilities that use these containers for intravenous medication preparation. Staff handling the containers during pharmacy operations are most at risk of spills or contamination.
Check for the model number H938905 on the container. These containers are used in intravenous admixture programs and come in 250ml or 1250ml sizes. Affected units have specific lot numbers listed in the recall notice.
Look for the model number H938905 and the specific lot numbers listed in the recall notice.
The Metrix recall states that these empty containers may leak, which could lead to medication spills or contamination during intravenous admixture preparation in pharmacies.
The recall does not specify a remedy, so contact Metrix directly for further instructions.
The containers are designed for use in pharmacies but may leak, so they should be checked for proper sealing before use.
We’ve drafted a message you can send Metrix to request your refund or repair — edit it as you like.
Subject: Recall Z-0008-2020 — Metrix Metrix Hello, I own a Metrix that is covered by recall Z-0008-2020 from Metrix. 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.
