B Braun recalls Microbore Extension Sets with 0.2 Micron Filter (V6215) due to incorrect label claiming air-eliminating filter when it does not have an air vent.
Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent, which is common to air eliminating filters.
B Braun is recalling Microbore Extension Sets with 0.2 Micron Filter (catalog number V6215) because the label incorrectly states the device contains an air-eliminating filter. This could lead to improper air management during IV treatments if the filter is not designed to remove air.
The product label claims the filter eliminates air, but the actual filter does not have an air vent, which is necessary for air elimination. This could cause air to accumulate in the IV line, potentially leading to air embolism if not properly managed.
Healthcare professionals using IV tubing with this specific Microbore Extension Set. Patients receiving IV treatments with the recalled product may be at risk if air is not properly managed.
Check for the catalog number V6215 on the product. The product was sold with lot numbers listed in the recall notice, including expiration dates from June 2025 through March 2029.
Look for the catalog number V6215 on the Microbore Extension Set with 0.2 Micron Filter.
The product label incorrectly states it contains an air-eliminating filter, but the actual filter does not have an air vent, which is necessary for air elimination.
The risk is that air may accumulate in the IV line if the filter is not designed to remove air, potentially causing air embolism in patients.
Check for the catalog number V6215 on the product. The product was sold with specific lot numbers listed in the recall notice, including expiration dates from June 2025 through March 2029.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2176-2025 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2176-2025 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.
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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.
