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Carefusion 2200 Inc recalls Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.
Recalled June 24, 2020 · FDA recall Z-2400-2020 · Carefusion 2200
Hazard
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. · FDA Class II
Units
358 units
Sold at
US Nationwide distribution including in the states of CA, FL, VA and KY.
Description
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.
Product
Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.
Manufacturer(s)
Carefusion 2200 Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →