B Braun Medical recalls SafeDAY IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units include specific catalog numbers and expiration dates.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical is recalling SafeDAY IV administration sets used with Infus: 1. IV ADMIN SET 60 DROP W/2 SAFEDAY with catalog number 352635. These sets can cause medication to flow backward into the main IV line and fail to prime properly, which may lead to incorrect dosing or complications.
The SafeDAY sets can allow medication from secondary IV containers to flow back into the primary IV line. This can cause incorrect dosing or blockages when the sets cannot be properly primed.
Healthcare professionals using these IV sets with Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for the catalog number 352635 on the SafeDAY set. These units were sold with Infusomat pumps like Space, Outlook, and Vista Basic models and expire 36 months from the start date.
Look for catalog number 352635 on the SafeDAY set label.
Reach out to B Braun Medical for guidance on next steps if you have the recalled set.
The recalled SafeDAY set is the IV ADMIN SET 60 DROP W/2 SAFEDAY with catalog number 352635.
Check for the catalog number 352635 on the set label. These units were sold with Infusomat pumps like Space, Outlook, and Vista Basic models and expire 36 months from the start date.
Contact B Braun Medical for guidance on next steps. The recall does not specify a return or replacement process.
We’ve drafted a message you can send B Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0711-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0711-2026 from B Braun Medical. 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.
