American Contract Systems recalls Diagnostic Neuro IR Tray Model WENE21 due to possible sterilization failure. This may cause treatment delays or prolonged procedures. Affected units include specific model numbers and production 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 Diagnostic Neuro IR Trays with model number WENE21 because they may not have been properly sterilized. This could lead to treatment delays or longer procedures for patients needing medical imaging.
The device may not have been properly sterilized during manufacturing, which could lead to contamination. This might cause treatment delays or prolonged procedures if the device is not functioning correctly.
Healthcare facilities using the Diagnostic Neuro IR Tray Model WENE21 are likely affected. Patients undergoing medical imaging procedures may be at risk if the device is not properly sterilized.
Check for model number WENE21 on the device. Affected units include specific production lots: 960241, 71-050727, 71-051234, 71-051771, 71-052322, 71-052501, 71-052705.
Look for model number WENE21 on the device to confirm if it is affected.
American Contract Systems is recalling Diagnostic Neuro IR Trays with model number WENE21 because they may not have been properly sterilized during manufacturing.
Possible loss or lack of functionality may lead to delays or prolonged treatment for patients needing medical imaging.
Check for model number WENE21 and production lots: 960241, 71-050727, 71-051234, 71-051771, 71-052322, 71-052501, 71-052705.
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-1354-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1354-2025 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.
