Carefusion 2200 Inc: Medical Device Recall in 2016 - (Recall #: Z-2212-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class I

Date Initiated: July 1, 2016

Date Posted: August 3, 2016

Recall Number: Z-2212-2016

Event ID: 74465

Reason for Recall:

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

Status: Terminated

Product Quantity: 10

Code Information:

Product Code 89-6114, Lot Code(s): 878971; 879366; 879404, and Date Code: C16

Distribution Pattern:

Worldwide Distribution - US, including the states of WA and MD; and, the country of Japan.

Voluntary or Mandated:

Voluntary: Firm initiated