Villa Sistemi Medicali S.P.A.: Medical Device Recall in 2017 - (Recall #: Z-1428-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Apollo; Models: 9784000131 9784000231 9784020131 9784020231 9784100231 9784120131 9784120231 9784130131 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.

Product Classification:

Class II

Date Initiated: December 27, 2016

Date Posted: March 15, 2017

Recall Number: Z-1428-2017

Event ID: 76367

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.

Status: Terminated

Product Quantity: 65 devices in total

Code Information:

Serial Numbers: 06100127 06110138 07010149 07020158 07020163 07020165 07030171 07040206 09010566 09090605 10100752 11100873 15041446

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated