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

Recall Z-0286-2025 — epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System, SMN 10736515

U.S. FDA — Device Enforcement · United States · 2024-09-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0286-2025
Date of alert
2024-09-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00809708121860
Reported risk: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium bias may exist in one lot of epoc BGEM BUN Test Cards approximately 2 months prior to expiration. The observed maximum negative bias from internal testing is -10 mmol/L. No positive bias has been observed. Quality Control (QC) fluid may or may not detect the issue depending on the bias magnitude and the frequency of QC testing. One customer complaint has been associated with this issue. No adverse events have been reported. All affected lots have recently expired before the issuance of the recall.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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.

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.