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

Recall Z-2400-2020 — Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.

U.S. FDA — Device Enforcement · United States · 2020-05-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2400-2020
Date of alert
2020-05-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Carefusion 2200 Inc
Product category
device
Product type
Devices
Reported risk: Becton Dickinson and Company, is conducting a voluntary recall on the V. MuellerTM 3H Knife Handles catalog number listed in the table above. BD has been informed by our supplier that the external threads on some of the collets (Figure 1) contain a machining burr, potentially causing the collet to not fully seat in the knife handle (Figure 2), inhibiting complete grip of the inserted knife blade possibly resulting in a loose blade.
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.