Remel recalls Thio Med w/o Ind w/Dex (9ml) 100/PK due to shortened expiration date from 9 months to 105 days after manufacturing, risking product failure 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 (9ml) 100/PK products because they may fail performance testing after 106 days of use. This means the expiration date is shortened from 9 months to 105 days, so users should check their product's lot number and expiration date to avoid potential testing failures.
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, meaning the product could become ineffective for use in cultivating aerobes and anaerobes.
Users of Thio Med w/o Ind w/Dex (9ml) 100/PK for qualitative procedures in labs or medical settings. Those who have the product with lot numbers listed in the recall are most at risk.
Check the lot number on the product label, which includes expiration dates like 11/26/2018 through 07/31/2019. The product is sold in packs of 100 units.
Look for lot numbers on the label that match the listed dates (e.g., 298271 to 423579) to determine if your product is affected.
The product may fail performance testing after 106 days from manufacturing, so the expiration date is shortened from 9 months to 105 days.
Lot numbers listed in the recall include 298271 (11/26/2018) through 423579 (07/31/2019).
Check the lot number on the product label; if it matches the listed dates (e.g., 298271 to 423579), your product is affected.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1400-2019 — Remel Remel Hello, I own a Remel that is covered by recall Z-1400-2019 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.
