American Contract Systems recalls laceration trays with model numbers SGLA07A, SGLA07B-0: possible sterilization failure may delay or prolong medical treatment. No remedy specified.
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 laceration trays with specific model numbers due to possible failure in sterilization assurance. This could lead to delays or prolonged treatment for patients using these medical devices.
The trays may not meet sterilization requirements, which could cause delays or longer treatment times for patients. This is not a direct safety hazard like a risk of injury or fire.
Patients using laceration trays with model numbers SGLA07A, SGLA07B-01, SGLA07B-02, or SGLA07B are most at risk. Healthcare facilities that use these trays may also be affected.
Check for model numbers SGLA07A, SGLA07B-01, SGLA07B-02, or SGLA07B on the tray. These were sold with specific lot numbers and UDI-DI codes listed in the recall notice.
Look for model numbers SGLA07A, SGLA07B-01, SGLA07B-02, or SGLA07B on the tray.
American Contract Systems is unable to confirm that the product met sterilization assurance requirements, which could lead to delays or prolonged treatment.
The recall does not specify a remedy, so no action is required beyond checking the model numbers.
The recall states possible delays or prolonged treatment, but no direct health risks like injury or infection are 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-1350-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1350-2025 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.
