Official recall record

Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.

US FDA — Medical Devices · 2025-07-09 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2025-07-09
Country of alert: United States
Alert level: Class I
Alert type: recall
Barcode (EAN/GTIN): 04046964189173
Brand on record: B BRAUN MEDICAL INC

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

Other recalls from this brand

All 41 official recall notices naming B. Braun Medical, Inc. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.