Pacific Medical Group recalls Aftermarket Alaris Infusion Pump Module Model 8100 Front
Pacific Medical Group recalls Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel components installed by their service team. Over time, posts may crack or separate, leading to free flow, over infusion, or under infusion. Affected units have serial numbers from 07/10/2020 to 02/18/2021.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
Pacific Medical Group is recalling aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel components that were installed during service. Over time, the posts on the bezel may crack or separate, which could cause free flow, over infusion, or under infusion of medication. This poses a risk of incorrect medication delivery. Read more at govinfonow.com/recall/62987-pacific-medical-group-recalls-aftermarket-alaris-infusion-pump-module-model.
Source Summary by GovInfoNow · govinfonow.com/recall/62987-pacific-medical-group-recalls-aftermarket-alaris-infusion-pump-module-model · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1375-2021
Cite this page
“Pacific Medical Group recalls Aftermarket Alaris Infusion Pump Module Model 8100 Front.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62987-pacific-medical-group-recalls-aftermarket-alaris-infusion-pump-module-model. Based on FDA recall #Z-1375-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1375-2021%22&limit=1).
Why it’s dangerous
Aftermarket front bezel components were installed during service by Pacific Medical Group (DBA Avante Health), not by the original manufacturer. Over time, the posts on the front bezel can crack or separate. If one or more posts separate, it could lead to free flow, over infusion, or under infusion of medication, which might cause incorrect medication delivery.
Who’s affected
Patients using infusion pumps with these specific aftermarket bezel components are at risk. Healthcare providers who installed the components during service may also be affected.
How to tell if you have this one
Check if your Alaris Infusion Pump Module Model 8100 has a front bezel installed by Pacific Medical Group (DBA Avante Health) between July 10, 2020 and February 18, 2021. Affected units have specific serial numbers listed in the recall.
- Brand
Trsmima- Category
Medical device
What to do — step by step
Check for affected serial numbers
Review the list of serial numbers provided in the recall to determine if your device is affected.
Contact Pacific Medical Group
Reach out to Pacific Medical Group for guidance on next steps if your device is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Distribution US nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1375-2021 (March 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1375-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.