Tenacore recalls Alaris Infusion Pump Module Model 8100 units serviced by Tenacor between July 2020 and February 2021 with specific serial numbers due to risk of infusion errors from cracked bezel repair parts.
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.
Tenacore is recalling Alaris Infusion Pump Module Model 8100 units that were serviced by Tenacor between July 2020 and February 2021. These pumps may have cracked bezel repair parts that could cause infusion errors like over-infusion or interruptions.
Bezel repair parts used by Tenacor to fix the pumps may crack or separate over time. This can cause the pump to over-infuse, under-infuse, or stop delivering medication, which could be dangerous for patients needing continuous treatment.
Users of Alaris Infusion Pump Module Model 8100 who had it serviced by Tenacor between July 10, 2020 and February 18, 2021 are affected. Patients using these pumps for medical treatment are at risk if the bezel repair parts crack.
Check if your Alaris Infusion Pump Module Model 8100 was serviced by Tenacor between July 10, 2020 and February 18, 2021. Look for specific serial numbers listed in the recall notice.
Verify if your pump has a serial number from the list provided in the recall notice.
If your pump is affected, contact Tenacor for further instructions on how to address the issue.
Bezel repair parts used by Tenacor to service the pumps may crack or separate over time, causing infusion errors like over-infusion or interruptions.
Check if your pump has a serial number from the list provided in the recall notice. If affected, contact Tenacor for further instructions.
Yes, pumps serviced by Tenacor between July 10, 2020 and February 18, 2021 are affected.
We’ve drafted a message you can send Tenacore to request your refund or repair — edit it as you like.
Subject: Recall Z-1331-2021 — Tenacore Tenacore Hello, I own a Tenacore that is covered by recall Z-1331-2021 from Tenacore. 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.
