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

Recall Z-0314-2024 — BLOOD CULTURE KIT, REF DYNDH1647B

U.S. FDA — Device Enforcement · United States · 2023-11-01 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0314-2024
Date of alert
2023-11-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
40195327267002
Reported risk: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
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.

Related

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.