American Contract Systems recalls General Angio Packs with specific model numbers due to unconfirmed sterilization. This may cause treatment delays or prolonged procedures. Affected units include model LLAP75G and variants.
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 General Angio Packs with model numbers LLAP75G and variants because they may not have been properly sterilized. This could lead to treatment delays or longer procedures for patients needing these medical devices.
The product may not have been properly sterilized during manufacturing. This could cause treatment delays or prolonged procedures if the device is not functioning correctly.
Patients using General Angio Packs for medical procedures are affected. Those with the specific model numbers listed in the recall are most at risk.
Check for model numbers LLAP75G, LLAP75G-01, LLAP75G-02, LLAP75G-03 on the device. The recall includes specific production lots and UDI-DI numbers listed in the notice.
Identify the model number on your General Angio Pack to see if it matches LLAP75G or the listed variants.
The recall is due to American Contract Systems being unable to confirm that the product met sterilization assurance requirements.
Possible treatment delays or prolonged procedures may occur if the device is not functioning correctly.
Check for model numbers LLAP75G, LLAP75G-01, LLAP75G-02, or LLAP75G-03 on the device.
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-1340-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1340-2025 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.
