Abbott recalls Alinity Reaction Vessels (REF: 06P1401) for use with Alinity i Systems and ARCHITECT systems due to potential contaminant affecting optical performance. No remedy specified in recall notice.
Reaction vessels may contain a potential contaminant that could affect their optical performance.
Abbott is recalling Alinity Reaction Vessels and ARCHITECT Reaction V:06P1401 models that may contain a contaminant affecting their optical performance. This could lead to inaccurate test results if used in medical testing systems.
The reaction vessels may contain a potential contaminant that could affect their optical performance. This might lead to inaccurate test results when used in medical testing systems, though the risk of serious injury is not described.
Healthcare facilities using Abbott's Alinity i Systems or ARCHITECT systems with these reaction vessels are most at risk. Patients receiving medical tests using these vessels could be affected if the contaminant causes inaccurate results.
Check for the model number REF: 06P1401 on the reaction vessels. These vessels are used with Abbott's Alinity i Systems and ARCHITECT systems. The UDI-DI/Lots numbers 00380740129026/000586790 and 000586879 are associated with this recall.
Look for the model number REF: 06P1401 on the reaction vessels.
The recall is due to a potential contaminant in the reaction vessels that could affect their optical performance, which might lead to inaccurate test results.
The recall does not specify a remedy, so no immediate action is required beyond checking if you have the affected model.
The official notice does not specify a remedy, so you do not need to take any action unless you have the affected model numbers.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-0958-2023 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-0958-2023 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.
