American Contract Systems recalls medical convenience kits with potential humidity issues that could affect sterilization. Learn if your kit is affected and what to do.
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 due to a problem with humidity readings that may mean the kits weren't properly sterilized. This could affect the safety of medical procedures using these kits.
The kit's chart recorder malfunctioned, causing humidity readings to be out of specification. This means ACS cannot confirm the kits were sterilized properly, which could lead to infection risks during medical procedures.
Healthcare providers using the Paracentesis Thoracente medical convenience kit (model SLPT76H) are most at risk. Patients undergoing procedures with this kit could be affected if sterilization is compromised.
Check for the model SLPT76H on the kit. The kit was sold with lot number 2405102 and expires May 10, 2025. The UDI-DI code is 00191072199065.
Look for the model number SLPT76H, lot number 2405102, and expiration date May 10, 2025 on the kit.
The manufacturer cannot confirm proper sterilization due to humidity issues, so it may not be safe for medical use.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
Check for the model SLPT76H, lot number 2405102, and expiration date May 10, 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-3234-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3234-2024 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.
