Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps

DEERFIELD, Ill. — Baxter International Inc. announced today it has initiated a voluntary recall of two lots of its Dual Luer Lock Caps (Product Code 2C6250, Lots 10043 and 10044) because of the presence of loose particulate matter found in the packaging. Particulate matter entering the fluid path from the Luer Lock Caps may result in thrombotic and embolic events, including: pulmonary embolism, myocardial infarction and stroke. There have been no reported complaints associated with this issue, however embolic events may not be easily attributed to such particulate matter. The root cause has been identified and resolved. The U.S. Food and Drug Administration (FDA) has designated this as a Class I recall.

Baxter’s Dual Luer Lock Cap is used as a protective cap on access ports on medical devices such as stopcocks or IV sets when not in use.

Customers should not use product from the two recalled lots and should locate and remove all affected product from their facility. Affected lots were distributed to customers between June 19, 2013, and August 20, 2013. Non-affected lot numbers can continue to be used according to the instructions for use. Affected lots should be returned to Baxter for credit by contacting Baxter Healthcare Center for Service at 1-888-229-0001 begin_of_the_skype_highlighting 1-888-229-0001 FREE  end_of_the_skype_highlighting between the hours of 7:00 a.m. and 6:00 p.m., Central Time. Unaffected lots of product code 2C6250 are available for replacement. Adverse reactions or quality problems can be reported to the FDA at http://www.fda.gov/Safety/medwatch/howtoreport/default.htm.
The financial impact of the recall is not material.

Read more here: http://www.heraldonline.com/2013/09/19/5226269/baxter-initiates-voluntary-recall.html#storylink=cpy