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Carefusion 2200 Inc recalls DIAMOND-FLEX CIRCULAR RETRACTOR, ANGLED, 40MM 5MM, Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date C
Recalled August 3, 2016 · FDA recall Z-2212-2016 · Carefusion 2200
Hazard
BD, formerly CareFusion, has identified a potential risk associated with a weld failure which could result in the wire protruding thru the tip of the instrument when articulated. If this failure were to occur while in use in a procedure it has the potential to damages tissue or organs · FDA Class I
Units
10
Sold at
Worldwide Distribution - US, including the states of WA and MD; and, the country of Japan.
Description
BD, formerly CareFusion, has identified a potential risk associated with a weld failure which could result in the wire protruding thru the tip of the instrument when articulated. If this failure were to occur while in use in a procedure it has the potential to damages tissue or organs
Product
DIAMOND-FLEX CIRCULAR RETRACTOR, ANGLED, 40MM 5MM, Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date Code: C16. Designed to retract or elevate organs and tissue to provide better visualization access.
Manufacturer(s)
Carefusion 2200 Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →