American Contract Systems recalls thoracic packs with model UTTC82Y/UTTC82AA-01 due to potential sterilization issues causing treatment delays. Affected units sold from specific lots.
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
American Contract Systems is recalling thoracic packs with model numbers UTTC82Y and UTTC8:82AA-01 because they may not have been properly sterilized. This could lead to treatment delays or complications for patients needing these medical devices.
The product may not have met sterilization requirements, which could cause treatment delays or prolonged medical procedures. This is not a safety hazard that could cause injury during normal use.
Patients using these thoracic packs for medical treatment are affected. Healthcare providers who use the product for procedures are most at risk of treatment delays.
Check for model numbers UTTC82Y or UTTC82AA-01 on the product. Affected units were sold with specific lot numbers: 954241, 921241, 889241, 70-051283, 70-052001, 70-052096, 70-053233.
Look for model numbers UTTC82Y or UTTC82AA-01 on the product.
The recall is due to possible failure to meet sterilization requirements, which could lead to treatment delays or prolonged medical procedures.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model numbers.
The hazard described is potential treatment delays, not a safety risk that could cause injury during normal use.
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-1361-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1361-2025 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.
