Remel recalls Thio Med w/o Ind w/Dex 18ml 100/PK due to shortened expiration date from 9 months to 105 days to prevent performance failures in testing.
Potential for products to fail performance testing per the Instructions for Use (IFU) starting at 106 days after date of manufacturing. Expiration date is shortened from 9 months to 105 days.
Remel is recalling Thio Med w/o Ind w/Dex (18ml) 100/pack products because they may fail performance testing after 106 days from manufacturing. This means the expiration date is shortened from 9 months to 105 days to ensure reliable results in qualitative procedures.
The product may fail performance testing after 106 days from manufacturing. This happens because the expiration date is shortened from 9 months to 105 days to prevent unreliable results in qualitative procedures.
Users of Thio Med w/o Ind w/Dex 18ml 100/pack for qualitative procedures are affected. Laboratory users handling these products are most at risk due to potential performance failures.
Check for lot numbers 314864 (12/24/2018), 343867 (02/14/2019), 367396 (04/02/2019), 387017 (05/09/2019), or expansion lot 423518 (07/30/2019) on the product label.
Verify the product's expiration date is within 105 days from manufacturing date to ensure reliable performance.
The expiration date is shortened from 9 months to 105 days to prevent performance failures in testing after 106 days from manufacturing.
The product may fail performance testing after 106 days from manufacturing, which could lead to unreliable results in qualitative procedures.
Look for lot numbers 314864 (12/24/2018), 343867 (02/14/2019), 367396 (04/02/2019), 387017 (05/09/2019), or expansion lot 423518 (07/30/2019) on the product label.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1408-2019 — Remel Remel Hello, I own a Remel that is covered by recall Z-1408-2019 from Remel. 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.
