Abbott recalls Alinity i Processing Module LN 03R65-01 due to potential safety interlock failure when removing bulk solution bottles from the Alinity i series. This could lead to unsafe conditions during use.
The safety interlock covering the septum piercing probes within the bulk solution bottle holder may not deploy when a bulk solution bottle is removed from the Alinity ci series and Alinity s System.
Abbott is recalling the Alinity i Processing Module LN 03R65-01 because the safety interlock covering the septum piercing probes might not deploy when a bulk solution bottle is removed. This could create unsafe conditions during use of the device.
The safety interlock mechanism that covers the septum piercing probes in the bulk solution bottle holder may fail to activate when a bulk solution bottle is removed from the Alinity i series device. This could allow the probes to be exposed without proper safety protection, potentially leading to unsafe conditions during use.
Users of the Alinity i Processing Module LN 03R65-01 who are performing blood tests with the Alinity i series device. Those handling the bulk solution bottles during testing are most at risk.
The Alinity i Processing Module LN 03R65-01 model. This product is used with the Alinity i series devices for blood testing. Check if you have this specific model number on your device.
Identify if your Alinity i Processing Module has the LN 03R65-01 model number.
If you have the recalled model, use the device with caution when removing bulk solution bottles to avoid potential safety interlock failure.
The recalled model is Alinity i Processing Module LN 03R65-01.
The safety interlock covering the septum piercing probes may not deploy when a bulk solution bottle is removed from the Alinity i series device, potentially creating unsafe conditions.
No, but you should use the device with caution when removing bulk solution bottles to avoid potential safety interlock failure.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1196-2019 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1196-2019 from Abbott. 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.
