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

HEMOCUE INC GLUC AQUEOUS 1HI/LO HEMCUE CONTROL KIT. — recall Z-1855-2025

U.S. FDA — Device Enforcement · United States · 2025-04-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1855-2025
Date of alert
2025-04-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mckesson Medical-Surgical Inc. Corporate Office
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
8718734960935
Reported risk: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
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.

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.