American Contract Systems recalls HIP SCOPE models CCHS21B and variants due to unconfirmed sterilization. This may cause treatment delays or reduced functionality. Affected units sold with specific serial numbers.
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 HIP SCOPE models because they may not have been properly sterilized. This could lead to treatment delays or reduced functionality for patients using the device.
The device may not have been properly sterilized during manufacturing. This could cause treatment delays or reduced functionality if the device is used without proper sterilization.
Patients using the HIP SCOPE device for medical treatments may be affected. Those with the specific model numbers and serial numbers listed are most at risk.
Check for model numbers CCHS21B, CCHS21B-01, or CCHS21B-02 on the device. Look for serial numbers 00191072193483, 962241, 914241, 70-050890, 70-051579, 70-052206, or 70-053085.
Identify the model number on the device to see if it matches CCHS21B, CCHS21B-01, or CCHS21B-02.
Check the serial number on the device to see if it matches the listed numbers.
American Contract Systems is unable to confirm that the device was properly sterilized, which could lead to treatment delays or reduced functionality.
The recall record does not specify a remedy, so no action is required unless you have the listed model or serial numbers.
Check for model numbers CCHS21B, CCHS21B-01, or CCHS21B-02 and serial numbers from the list provided in the recall.
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-1333-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1333-2025 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.
