American Contract Systems recalls VEIN TRAY models UTVT21C and variants due to possible sterilization issues affecting treatment safety. Affected units may cause delays or complications in medical procedures.
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 certain VEIN TRAY models because they may not have been properly sterilized. This could lead to delays or complications in medical treatments if the trays are used without proper sterilization.
The trays may not have been properly sterilized during manufacturing, which could lead to contamination. This contamination risk might cause treatment delays or complications if the trays are used without adequate sterilization.
Healthcare professionals using the recalled VEIN TRAY models for medical procedures are most at risk. Patients receiving treatments with these trays may experience delays or complications.
Check for model numbers UTVT21C, UTVT21C02, or UTVT21C-03 on the tray. The recall includes units with specific lot numbers: 70-051418, 70-052083, and 70-052850.
Look for model numbers UTVT21C, UTVT21C02, or UTVT21C-03 on the tray.
American Contract Systems cannot confirm that the trays were properly sterilized, which could lead to delays or complications in medical treatments.
The recall record does not specify a remedy, so no action is required beyond checking the model number.
Yes, the affected units include lot numbers 70-051418, 70-052083, and 70-052850.
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-1362-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1362-2025 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.
