Abbott recalls Alinity c Processing Module LN 03R67-01 due to potential safety interlock failure when removing bulk solution bottles, which could lead to improper operation.
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 c Processing Module LN 03R67-01 because the safety interlock mechanism might not activate when removing bulk solution bottles. This could cause improper operation of the device, though serious injury risks are not explicitly stated.
The safety interlock covering the septum piercing probes may not deploy when a bulk solution bottle is removed from the Alinity c series and Alinity s System. This could lead to improper operation of the device if the interlock fails to activate.
Users of the Alinity c Processing Module LN 03R67-01 for laboratory testing. Healthcare professionals and lab technicians who operate this device are most at risk.
The Alinity c Processing Module LN 03R67-01 model. This device is used in laboratory settings for automated chemistry analysis and is part of Abbott's Alinity c series.
Verify if your Alinity c Processing Module is model LN 03R67-01 by checking the device label or documentation.
The safety interlock covering the septum piercing probes may not deploy when a bulk solution bottle is removed from the Alinity c series and Alinity s System.
The recall record does not specify a risk of serious injury; it only mentions potential improper operation.
Check if your Alinity c Processing Module is model LN 03R67-01, as this specific model is recalled.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1197-2019 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1197-2019 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.
