Immunostics recalls Detector H. Pylori (IHP-30) with incorrect expiration date labels. Using expired products may cause false test results. Affected lots: 0821132-2 to 0821132-4.
Labeling for affected lots incorrectly indicates the expiration date is 10/31/2023. However, the correct expiration date is 10/31/2022. Use of the product after its expiration may cause false positive, false negative, or invalid results.
Immunostics is recalling its Detector H. Pylori test kits because the expiration date labels are incorrect. Using these kits after the actual expiration date (October 31, 2022) could lead to false positive or false negative results, making tests unreliable.
The test kits have labels that incorrectly show an expiration date of October 31, 2023, when the actual expiration is October 31, 2022. Using the product after its true expiration date may cause the test to give inaccurate results, such as false positives or false negatives.
People who own or use Immunostics Detector H. Pylori test kits with lot numbers 0821132-2 through 0821132-4 are affected. Those who rely on these tests for accurate results are most at risk.
Check the label on the test kit for the expiration date. Affected lots have the label 'Expiration: 2023-10-31' but the correct expiration is 2022-10-31. Lot numbers 0821132-2 to 0821132-4 are affected.
Look for the label that says 'Expiration: 2023-10-31' on the test kit. If present, this kit is affected.
The label incorrectly shows an expiration date of October 31, 2023, when the actual expiration is October 31, 2022.
Using the product after its true expiration date (October 31, 2022) may cause false positive or false negative results.
Lots 0821132-2, 0821132-3, and 0821132-4 are affected.
We’ve drafted a message you can send Immunostics to request your refund or repair — edit it as you like.
Subject: Recall Z-0702-2024 — Immunostics Immunostics Hello, I own a Immunostics that is covered by recall Z-0702-2024 from Immunostics. 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.
