Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mueller Knife Handle Recalled by Carefusion 2200 Inc Due to Becton Dickinson and Company, is conducting a voluntary...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Carefusion 2200 Inc directly.
Affected Products
Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.
Quantity: 358 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carefusion 2200 Inc
Carefusion 2200 Inc has 112 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report