Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
DIAMOND-FLEX CIRCULAR RETRACTOR Recalled by Carefusion 2200 Inc Due to BD, formerly CareFusion, has identified a potential risk...
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
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.
Quantity: 10
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed to 2 states: MD, WA
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