Z-2400-2020 Class II Terminated
FDA device recall Z-2400-2020 was initiated by Carefusion 2200 Inc on May 18, 2020 and is designated Class II. Reason for recall: 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 thr… The recall status is terminated (terminated April 25, 2021). Affected quantity: 358 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 24, 2020
- Initiation Date
- May 18, 2020
- Termination Date
- April 25, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 358 units
Product Description
Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.
Reason for Recall
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.
Distribution Pattern
US Nationwide distribution including in the states of CA, FL, VA and KY.
Code Information
Model Numbers: OP0702 and OP0703. Model OP0702, Lot C20VAA ( 4 inch length) Model OP0703, Lot D17VAA (6 inch length)