American Contract Systems recalls AV FISTULA Model UTAV77T due to unconfirmed sterilization. This may cause treatment delays or reduced functionality. Check product details for affected units.
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 AV FISTULA Model UTAV77T because they can't confirm it was properly sterilized. This could lead to treatment delays or problems with the device's function.
The device may not be properly sterilized, which could cause treatment delays or reduced functionality. This means the device might not work as intended during medical procedures.
Patients using AV FISTULA devices for medical treatments may be affected. Those with the specific model number or lot codes listed are most at risk.
Check for the model number UTAV77T and lot codes 961241, 890: 70-051326, 70-051979, or 70-053058 on the device or packaging.
Look for the model number UTAV77T and lot codes 961241, 890241, 70-051326, 70-051979, or 70-053058 on the device or packaging.
American Contract Systems cannot confirm the device was properly sterilized, which may cause treatment delays or reduced functionality.
Check the product details for the model number UTAV77T and lot codes listed. If you have the affected device, contact American Contract Systems for further instructions.
The recall states possible treatment delays or reduced functionality, but no specific injury risk is mentioned.
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-1356-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1356-2025 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.
