American Contract Systems recalls Shoulder medical kits with faulty humidity sensors that may not meet sterilization standards. Affected units have specific lot and expiration details.
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 that may not properly sterilize due to humidity sensor issues. This could mean the kits don't meet safety requirements for medical use.
The humidity sensor in the kit is inoperable, causing humidity readings to be out of specification. This means the product cannot confirm that sterilization requirements were met, potentially affecting medical safety.
Medical facilities using the Shoulder medical convenience kits with the specific lot number 2405112 and expiration date 05/11/2025 are most at risk. Healthcare workers using these kits for patient care may be affected.
Check for the model SESH18I and lot number 2405112 on the kit. The expiration date is May 11, 2025. This recall applies to medical convenience kits sold by American Contract Systems.
Look for the model SESH18I and lot number 2405112 on the medical convenience kit.
The humidity sensor is inoperable, causing humidity readings to be out of specification and preventing confirmation of sterilization requirements.
The recall record does not specify a remedy, so no action is required beyond checking the kit details.
The recall indicates the kit may not meet sterilization standards, so it is not safe for medical use without confirmation of proper sterilization.
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-3232-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3232-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
