American Contract Systems recalls medical convenience kits with faulty humidity sensors that may not meet sterilization standards. Affected units have specific model and lot numbers.
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 medical convenience kits because a faulty humidity sensor could mean the product doesn't meet sterilization requirements. This affects kits that were sold with specific model and lot numbers.
The humidity sensor in the kit is inoperable, which means the device can't accurately measure humidity levels. This leads to uncertainty about whether the product has been properly sterilized, which is critical for medical use.
Medical professionals using the Cysto medical convenience kits with model FTCY03L and lot number 2405033 are most at risk. The recall applies to kits sold between 2023 and 2025.
Check for the model number FTCY03L and lot number 2405033 on the kit. The kit was sold with an expiration date of May 3, 2025.
Look for the model number FTCY03L and lot number 2405033 on the kit.
The humidity sensor is inoperable, which means the device can't confirm proper sterilization, potentially affecting medical safety.
The recall record doesn't specify a remedy, so check the kit details and contact American Contract Systems for further instructions.
The recall indicates potential sterilization issues, but no specific injury risk is mentioned in the record.
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-3243-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3243-2024 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.
