Class II — B. Braun Medical, Inc.
| Recalling firm | B. BRAUN MEDICAL INC. |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for leakage at the joint between the blood filters and tubing |
| Product | Safeline Y-Type Blood Set, Catalog Number NF5140 |
| Quantity | 3,300 units |
| Distribution | US Nationwide |
| Initiated | 2019-11-20 |
| Classified | 2020-02-01 |
| Terminated | 2020-10-16 |
| Recall number | Z-0940-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — B. Braun Medical, Inc. (Z-0940-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84365/
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