B. Braun recalls EPID trays with catalog #339186 due to potential filter membrane damage causing inadequate filter capacity. Affected units sold between 2018-2019.
The filter capacity is not achieved due to damage of the filter membrane.
B. Braun is recalling certain EPID trays that may have damaged filter membranes, which could lead to inadequate filtration. This poses a risk of contamination during medical procedures if the tray is used without proper filtration.
The filter membrane in these trays may be damaged, reducing the tray's ability to filter contaminants effectively. This could lead to inadequate filtration during medical procedures if the tray is used without proper filtration.
Healthcare facilities using the recalled EPID trays with catalog number 339186 are most at risk. Patients undergoing procedures using these trays could potentially be exposed to contaminants.
Check for catalog number 339186 on the tray. The recall includes units with lot numbers 0061536043 (expiring 8/31/2018) and 0061620273 (expiring 11/30/2019).
Verify the catalog number and lot numbers on the tray to confirm if it's affected.
The recall indicates potential filter membrane damage that could reduce filtration effectiveness, but the official notice does not specify a risk of serious injury.
Check for catalog number 339186 and lot numbers 0061536043 (expiring 8/31/2018) or 0061620273 (expiring 11/30/2019).
The recall does not specify a remedy, so the official notice does not provide instructions for action.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2470-2019 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2470-2019 from B. Braun. 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.
