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

Recall Z-2466-2019 — ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114

U.S. FDA — Device Enforcement · United States · 2019-07-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2466-2019
Date of alert
2019-07-10
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)
0061537250
Reported risk: The filter capacity is not achieved due to damage of the filter membrane.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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