RegWardenFDA facility compliance records
Recall

Class I — Elite Biomedical Solutions LLC

Recalling firmElite Biomedical Solutions LLC
Registered facilityElite Biomedical Solutions LLC (the firm's only registered facility)
ClassificationClass I
StatusTerminated
ReasonAdministration of inappropriate quantities of fluid can result, with the potential to cause injury or death.
ProductAlaris Medley LVP Frame Membrane. 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.
Quantity609 pieces
DistributionNationwide 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.
Initiated2015-06-03
Classified2015-08-19
Terminated2017-03-07
Recall numberZ-2371-2015
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class I recall — Elite Biomedical Solutions LLC (Z-2371-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71543/

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