Medical device recalls High risk

Elite Biomedical Solutions LLC recalls Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal c…

Recall date
June 3, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2372-2015
FDA classification
Class I
Brand / firm
Elite Biomedical Solutions LLC
Sold / distributed
Nationwide Distribution in the states of AZ, CA, GA, IL, IN, KS, KY, MA, MD, MN, MO, MS, NC, NY, OH, PA, SC, TN, TX, VA & WI.

Why it was recalled

Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.

Get recall alerts

Free email alert whenever Elite Biomedical Solutions LLC has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Elite Biomedical Solutions LLC