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ECRI Institute Issues Priority Alert About Two Infusion Pumps
Date:5/28/2008

Recommends Curlin Medical's CMS and PainSmart Infusion Pumps Undergo Immediate Testing to Prevent Potential Life-Threatening Medication Overinfusion

PLYMOUTH MEETING, Pa., May 28 /PRNewswire-USNewswire/ -- ECRI Institute (http://www.ecri.org), an independent, nonprofit organization that researches the best approaches to improving patient care, has issued a priority medical device alert on its Web site, http://www.ecri.org/PatientSafety/Pages/safetyresources_pages_default.aspx, recommending immediate volume testing of Curlin Medical's (http://www.curlinmedical.com/home) 2000 CMS(TM), 4000 CMS(TM), 6000 CMS(TM), and PainSmart(TM) series pumps for potential overinfusion of medications. The pumps are used in hospitals and home healthcare settings.

Engineers at ECRI Institute's medical device laboratory tested Curlin pumps and found that doors on the pumps do not fully compress tubing during operation, which may result in intermittent gravity flow, releasing medication too quickly. ECRI Institute emphasizes that there may be no visible indication that a pump permits gravity flow and that volume testing is the only way to determine whether a particular pump has a door problem.

"In addition to immediately identifying and testing all Curlin pumps, we recommend instituting a policy of regular volume testing every three months," says Eric S. Sacks, Director, Healthcare Product Alerts, ECRI Institute.

Alerts are issued weekly in Health Devices Alerts, a component of membership in ECRI Institute's Health Devices System, Health Devices Gold, and SELECTplus(TM) programs. Each alert includes a priority level, problem summary, perspectives, and recommendations for responding to the problem.

Full access to the May 22, 2008, priority
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SOURCE ECRI Institute
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