Recall Atlas
Drugs & medicalClass II

ZIEHM-ORTHOSCAN INC recalls Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020

The accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure from the cart.

Read the official notice →
Date
2026-11-04
Country
United States
Brand
ZIEHM-ORTHOSCAN INC
Product
Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AZ , CA , CO , CT , FL…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

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  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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