26-Lead Transfer Set for use with APEX¿ Compounding System — Class II medical device recall Z-2343-2018
Terminated recall by B. Braun Medical, Inc., reported 2018-07-11, distributed in AL, CA, CO, CT, FL, GA, IL, LA…. There is a potential for valves on the 26-Lead Transfer Set to be incorrectly oriented. When a transfer set wi
| Recall number | Z-2343-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | B. Braun Medical, Inc., Allentown, PA, United States |
| Recall initiated | 2018-06-04 |
| Classified | 2018-07-03 |
| Reported by FDA | 2018-07-11 |
| Terminated | 2020-01-13 |
| Distributed | AL, CA, CO, CT, FL, GA, IL, LA, MA, MD, MI, MN, MO, NC, NJ, NV, OH, PA, TX, WA |
| Quantity | 12,320 |
| Model numbers | 2112550 |
Product
26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
Reason for recall
There is a potential for valves on the 26-Lead Transfer Set to be incorrectly oriented. When a transfer set with an incorrectly oriented valve is installed on the system, there is potential for unintended admixture.
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-2343-2018. 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.