American Contract Systems recalls Nasal Sinus Pack MTSN26B due to humidity readings out of spec, risking unconfirmed sterilization. Affected units sold from 2024 to 2025.
ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
American Contract Systems is recalling Nasal Sinus Packs with model MTSN26B because humidity readings in the medical kit were out of specification. This means the product's sterilization cannot be confirmed, which could lead to infection risks if used improperly.
The medical kit's humidity readings were out of specification due to an inoperable chart recorder. This prevents American Contract Systems from confirming that the product was properly sterilized, which could lead to infection if the kit is used without adequate sterilization.
Medical users who purchased the Nasal Sinus Pack MTSN26B model between 2024 and 2025 are affected. Healthcare providers and patients using this kit for nasal sinus treatments are most at risk.
Check for the model number MTSN26B on the Nasal Sinus Pack. The kit was sold with lot number 2405093 and expires May 9, 2025.
Identify the model number MTSN26B and lot number 2405093 on the kit.
The product's humidity readings were out of specification due to an inoperable chart recorder, preventing confirmation of proper sterilization.
The recall record does not mention any remedy or fix for this product.
The product was sold with lot number 2405093 and expires May 9, 2025.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-3242-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3242-2024 from American Contract Systems. 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.
