Metrix recalls SECURE EVA Dual Chamber Containers (REF 66641) for potential leaking product in intravenous admixture use. Affected units include specific Canadian lot numbers.
Potential for leaking product
Metrix is recalling SECURE EVA Dual Chamber Containers with Manifold (4000mL, REF 66641) due to a potential risk of leaking product. This could affect intravenous admixture storage and delivery in pharmacies.
The container is designed for intravenous parenteral admixtures in pharmacy settings. Leaking could occur during normal use, potentially contaminating the admixture or causing product waste.
Pharmacies using the SECURE EVA Dual Chamber Container with Manifold (4000mL, REF 66641) in Canada are likely affected. Healthcare workers handling intravenous admixtures are at risk if the container leaks.
Check for the model number REF 66641 with lot numbers: 66641-A2630, 66641-A2683, 66641-A3005, 66641-A3560, 66641-A3796, 66641-A3979, 66641-A4220, 66641-A4473, 66641-A4543, 66641-A5066, 66641-A5283, 66641-A5412, 66641-A5556, 66641-A5671. These units were sold in Canada.
Look for the lot numbers listed: 66641-A2630 through 66641-A5671 on the container.
The recall is for potential leaking product during intravenous admixture storage and delivery in pharmacy settings.
The recall record does not specify a remedy, so no action is required beyond checking the lot number.
The container is designed for safe use in pharmacy settings, but the recall indicates a potential risk of leaking.
We’ve drafted a message you can send Metrix to request your refund or repair — edit it as you like.
Subject: Recall Z-0006-2020 — Metrix Metrix Hello, I own a Metrix that is covered by recall Z-0006-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
