American Contract Systems recalls URO ROBOTIC PACK models LVUR44C and LVUR44C-03 due to possible sterilization issues causing treatment delays. Affected units sold from 2022-2023.
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 URO ROBOTIC PACK models LVUR44C and LVUR44C-03 because they may not meet sterilization requirements, which could delay or prolong medical treatments. This recall affects users who rely on these devices for healthcare.
The product may not meet sterilization requirements, which could lead to treatment delays or prolonged medical procedures. This happens because the device might not be properly sterilized during manufacturing, affecting its safety for medical use.
Users of the URO ROBOTIC PACK for medical treatments are affected. Those with ongoing treatments using these devices are most at risk of delayed care.
Check for model numbers LVUR44C or LVUR44C-03 on the device. Units sold between 2022 and 2023 with UDI-DI codes 00191072136688 are affected.
Look for model numbers LVUR44C or LVUR44C-03 on the device.
The recall is due to possible failure to meet sterilization requirements, which could cause treatment delays or prolonged medical procedures.
Check for model numbers LVUR44C or LVUR44C-03 and UDI-DI code 00191072136688. Units sold between 2022 and 2023 are affected.
The recall does not specify a remedy, so contact American Contract Systems for guidance.
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-1345-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1345-2025 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.
