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

Recall Z-0965-2024 — MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A

U.S. FDA — Device Enforcement · United States · 2023-12-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0965-2024
Date of alert
2023-12-21
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)
40195327347551
Reported risk: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
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.