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.
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.
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.
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.
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.
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.
Review the list of serial numbers provided in the recall to determine if your device is affected.
Reach out to Pacific Medical Group for guidance on next steps if your device is affected.
If the posts on the front bezel crack or separate, it could lead to free flow, over infusion, or under infusion of medication, which might cause incorrect medication delivery.
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.
Contact Pacific Medical Group for guidance on next steps if your device is affected.
We’ve drafted a message you can send Trsmima to request your refund or repair — edit it as you like.
Subject: Recall Z-1375-2021 — Trsmima Trsmima Hello, I own a Trsmima that is covered by recall Z-1375-2021 from Trsmima. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
