American Contract Systems recalls MAJOR DIEP models CCMJ73G-01 and CCMJ7: Possible treatment delays due to unconfirmed sterilization. Return or stop use to avoid risks.
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 two specific MAJOR DIEP models because they may not have been properly sterilized. This could cause delays or longer treatment times for users. The recall is for specific model numbers and serial ranges.
The devices may not have been properly sterilized during manufacturing. This could lead to treatment delays or prolonged therapy if the device isn't functioning correctly.
Users of the MAJOR DIEP models CCMJ73G-01 and CCMJ73H are affected. Patients receiving medical treatments with these devices are most at risk.
Check for model numbers CCMJ73G-01 or CCMJ73H on the device. The serial numbers 00191072222824 to 00191072223890 are also part of this recall.
Look for model numbers CCMJ73G-01 or CCMJ73H on the device.
Reach out to American Contract Systems for further instructions on the recall.
The recall is because American Contract Systems cannot confirm that the devices were properly sterilized, which could lead to treatment delays or prolonged therapy.
The affected models are MAJOR DIEP with model numbers CCMJ73G-01 and CCMJ73H.
Check for model numbers CCMJ73G-01 or CCMJ73H and serial numbers 00191072222824 to 00191072223890.
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-1334-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1334-2025 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.
