Toshiba American Medical Systems Inc: Medical Device Recall in 2018 - (Recall #: Z-0842-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

INFX-8000F Fluoroscopic X-Ray Systems

Product Classification:

Class II

Date Initiated: December 29, 2017

Date Posted: March 14, 2018

Recall Number: Z-0842-2018

Event ID: 79153

Reason for Recall:

During an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the ceiling drive loosened cause the error.

Status: Terminated

Product Quantity: 17 units

Code Information:

Serial Numbers: AHA1592004, AGB1482001, AHA1482001, AGA1492002, AHA14Z2002, AGA1552003, UUB13Y2039, AHA15Y2005, AHA1612006, AHB1662007, AGB1682004, AGB1692005, AGB16Z2006, AHB1712008, AHB1712009, AGB1712007, AHA1582003

Distribution Pattern:

United States

Voluntary or Mandated:

Voluntary: Firm initiated