Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by Pacific Medical Group Inc. Due to Aftermarket front bezel components were installed during service/repair,...
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 Pacific Medical Group Inc. directly.
Affected Products
Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (DBA Avante Health Solutions)
Quantity: 2452
Why Was This Recalled?
Aftermarket front bezel components were installed during service/repair, not by the original manufacturer, within infusion pump modules. Over time, the posts on the front bezel component may crack or separate. Separation of one or more bezel posts could lead to free flow, over infusion, under infusion, or interruption of infusion.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pacific Medical Group Inc.
Pacific Medical Group Inc. has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report