Stimuplex A — Class II medical device recall Z-2132-2024
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-2132-2024 |
|---|---|
| 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 | 1,783,991 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04022495101211 |
| Lot numbers | 19E11, 19E14, 19E15, 19E16, 19E30, 19E31, 19F04, 19F05, 19F07, 19F21, 19F22, 19F26, 19F27, 19F28, 19F29, 19G30, 19H01, 19H02, 19H07, 19H08, 19H31, 19I04, 19I06, 19I07, 19K01, 19K02, 19K04, 19K08, 19K09, 19K27, 19K30, 19L06, 19L07, 19M05, 19M07, 19M10, 20A09, 20A11, 20A15, 20A17 and 237 more |
| Model numbers | 4894260 |
Product
Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
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-2132-2024. 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.