Product Wiki · Recalls · U.S. FDA — Device Enforcement

26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550 — recall Z-2343-2018

U.S. FDA — Device Enforcement · United States · 2018-06-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2343-2018
Date of alert
2018-06-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
B. Braun Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0061546906
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.