Stimuplex A — Class II medical device recall Z-2131-2024
Ongoing recall by B Braun Medical Inc, reported 2024-06-19, distributed nationwide. The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces o
| Recall number | Z-2131-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | B Braun Medical Inc, Breinigsville, PA, United States |
| Recall initiated | 2024-05-17 |
| Classified | 2024-06-11 |
| Reported by FDA | 2024-06-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 20,850 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04022495101167 |
| Lot numbers | 19L09, 19L27, 20A19, 20E15, 20H21, 21G14, 21I16, 22H23 |
| Model numbers | 4894251 |
Product
Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
Reason for recall
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2131-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.