Class II — B Braun Medical Inc
| Recalling firm | B. BRAUN MEDICAL SAS |
|---|---|
| Registered facility | B. BRAUN MEDICAL (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP. |
| Product | Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260 |
| Quantity | 1,783,991 units |
| Distribution | Worldwide distribution - US Nationwide and the country of Canada. |
| Initiated | 2024-05-17 |
| Classified | 2024-06-11 |
| Recall number | Z-2132-2024 |
| 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-2132-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94637/
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