FDA Class 2 Recall: Radiography 7000 M and OmniaSecure Devices

The most useful fact for most readers is simple: the U.S. Food and Drug Administration (FDA) has posted Class 2 device recalls for two products, Radiography 7000 M and OmniaSecure. If you use, own, or work with either device, the next step is to check the official FDA recall pages to confirm whether your specific model or unit is covered.

A Class 2 recall is a category the FDA uses for devices that may cause temporary or medically reversible health problems, or where the chance of serious harm is low. This post does not offer legal or medical advice. If you have questions about your health or a device you use, talk to a qualified professional.

What was recalled

The source material for this post is two FDA recall listings. One is titled “Class 2 Device Recall Radiography 7000 M.” The other is titled “Class 2 Device Recall OmniaSecure.” Those titles are the confirmed facts here.

The headlines do not include the full recall notices. Details such as the exact model numbers, lot or serial numbers, the reason for each recall, the number of units affected, and the dates involved are not in the source material. Rather than guess, this post points you to the official pages where those details are published.

Who should check

Anyone who uses, owns, stores, or services a device labeled Radiography 7000 M should check the FDA listing. The same applies to anyone connected to a device labeled OmniaSecure.

That includes clinics, imaging facilities, technicians, biomedical staff, and anyone who manages device inventory. If you are not sure whether a device you have is the one named, the official recall page is the place to confirm it. Do not rely on a headline alone.

What the recall notice will tell you

FDA device recall listings usually explain which products are affected and what action the company is asking customers to take. The exact instructions for these two recalls are not included in the source material, so check the official pages for the details.

When you open each listing, look for the model list, the affected lot or serial numbers, the reason for the recall, and any instructions on stopping use, returning the device, or arranging a correction. If something on the page is unclear, contact the device maker or your supplier using the contact details in the notice.

What to do now

• Open the two FDA recall links in the Sources section below.
• Check the model list on each official recall page to see if your device is covered.
• If your device matches, follow the instructions in the official notice.
• Record the model and serial number of your device before you contact anyone.
• Share the official notice with whoever services or manages the device.

StillOwed is not affiliated with any government agency. This post summarizes public recall listings in plain English and does not replace the official notices.

Sources

U.S. Food and Drug Administration (.gov): Class 2 Device Recall Radiography 7000 M

U.S. Food and Drug Administration (.gov): Class 2 Device Recall OmniaSecure