American Contract Systems recalls laceration trays with model numbers SGLA07A, SGLA07B-0: possible sterilization failure may delay or prolong treatment. No remedy specified in recall notice.
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 the trays.
The trays may not be properly sterilized, which could lead to contamination or infection risks. This might cause treatment delays or prolonged healing for patients needing the trays.
Healthcare professionals and patients who use the recalled laceration trays for wound care may be affected. Those using the trays for medical procedures are at risk of treatment delays.
Check for model numbers SGLA07A, SGLA07B-01, SGLA07B-02, or SGLA07B on the trays. The recall includes specific lot numbers and UDI-DI codes listed in the notice.
Identify the model number on the tray to see if it matches SGLA07A, SGLA07B-01, SGLA07B-02, or SGLA07B.
The recall is due to possible failure in sterilization assurance, which could lead to delays or prolonged treatment.
The recall notice does not specify a remedy, so no action is required beyond checking the model number.
The recall states possible delays or prolonged treatment, 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-1349-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1349-2025 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.
