Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Alaris Infusion Pump Module Recalled by BioMedical Equipment Service Co (BMES) Due to Bezel repair parts used, not by the original...
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 BioMedical Equipment Service Co (BMES) directly.
Affected Products
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted bezel repair part TIPA-8100-4410
Quantity: 718 potentially affected pumps
Why Was This Recalled?
Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.
Where Was This Sold?
This product was distributed to 9 states: CA, IL, IN, KY, LA, NV, NJ, OH, PA
About BioMedical Equipment Service Co (BMES)
BioMedical Equipment Service Co (BMES) has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report