Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of ...

FDA Recall #Z-1430-2017 — Class II — December 27, 2016

Recall #Z-1430-2017 Date: December 27, 2016 Classification: Class II Status: Terminated

Product Description

Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures

Reason for Recall

Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.

Recalling Firm

Villa Sistemi Medicali S.P.A. — Buccinasco, N/A

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

65 devices in total

Distribution

US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA, Puerto Rico, TN, TX, UT, and W.I

Code Information

Serial Number: 13101261

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated