Drug recall
26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
FDA recall event 80231 · Class II · B. Braun Medical, Inc.
Key facts
| Event ID | 80231 |
|---|---|
| Recall numbers | Z-2343-2018 |
| Recalling firm | B. Braun Medical, Inc. |
| Product type | Devices |
| Products | 26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Jun 4, 2018 |
| Report date | Jul 11, 2018 |
| Termination date | Jan 13, 2020 |
| City | Allentown |
| State | PA |
| Country | United States |
| FEI number | 2523676 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: