Medline recalls Primary Warmer Packs with Vyaire enFlow cartridges due to potential unsafe aluminum levels in infusion sets, risking serious patient injury.
The Vyaire enFlow disposable cartridge was recalled due to the potential for unsafe aluminum levels to elute into the infusate. The Use of the BD Alaris Pump Infusion Set may lead to serious adverse events for patients due to the incomplete occlusion caused by variation in tubing wall thickness.
Medline is recalling Primary Warmer Packs that contain Vyaire enFlow disposable cartridges because they may release unsafe aluminum levels into patient fluids. This could cause serious health issues for patients receiving IV treatments.
The Vyaire enFlow disposable cartridges may release unsafe aluminum levels into patient fluids during IV treatments. This can lead to serious health issues if the aluminum levels become too high, especially for patients with compromised health.
Patients using IV treatments with the recalled warmer packs are at risk. Healthcare providers who use these packs for patient warming should check if their equipment is affected.
Look for Medline Primary Warmer Packs with Product Number DYNJ52510A. The affected cartridges were sold in specific lots from 2018 to 2019.
Identify the lot number on the warmer pack, which may be found on the packaging or label.
Reach out to Medline directly to request a replacement or alternative solution for the affected warmer packs.
The Vyaire enFlow disposable cartridges may release unsafe aluminum levels into patient fluids, which can cause serious health issues for patients receiving IV treatments.
Look for Medline Primary Warmer Packs with Product Number DYNJ52510A, which were sold in specific lots from 2018 to 2019.
Contact Medline directly to request a replacement or alternative solution for the affected warmer packs.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2066-2019 — Medline Medline Hello, I own a Medline that is covered by recall Z-2066-2019 from Medline. 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.
