Abbott recalls Technopath Multichem S Plus Level 2 due to delivery without required dry ice, which may affect lab testing accuracy. Affected units include specific lot numbers.
Devices were delivered without the required dry ice.
Abbott is recalling Technopath Multichem S Plus Level 2 lab test kits because they were shipped without the necessary dry ice. This could lead to inaccurate lab results if used without proper cooling.
The test kits require dry ice to stay properly cooled during shipping. Without dry ice, the kits may not function correctly, leading to inaccurate lab results. This does not pose an immediate physical danger but affects test reliability.
Lab technicians and healthcare facilities using the Technopath Multichem S Plus Level 2 test kits. Those who have the specific lot number 18005182 are most at risk.
Check for the lot number 18005182 on the packaging. The product is a lab test kit for quality control in medical testing procedures.
Look for lot number 18005182 on the packaging to confirm if the item is affected.
The recall record states that devices were delivered without the required dry ice.
The recall record does not specify a remedy, so check the lot number 18005182 to see if it's affected.
The recall indicates a risk of inaccurate lab results, but it does not pose a physical danger like injury or fire.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1363-2019 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1363-2019 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.
