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

Recall Z-3069-2024 — CRANIOTOMY PACK, Pack Number DYNJ46552O

U.S. FDA — Device Enforcement · United States · 2024-06-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3069-2024
Date of alert
2024-06-18
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)
40195327467044
Reported risk: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.