Villa Sistemi Medicali S.P.A.: Medical Device Recall in 2017 - (Recall #: Z-1429-2017)

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 DRF; Model: 9784220831 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-1429-2017

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:

08090531 09090591 10040680 15051450 11020798

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