FUJIFILM Healthcare Americas Corporation: Device Recall

Recall Details

Recall Number

Z-1407-2025

Classification

Class II

Product Type

Device

Recalling Firm

FUJIFILM Healthcare Americas Corporation

Status

Ongoing

Date Initiated

02/11/2025

Location

Lexington, MA, United States

Voluntary/Mandated

Voluntary: Firm initiated

Product Quantity

104 units (69 US, 35 OUS)

Reason for Recall

The incorrect computed patient age is showing in VX for patients less than 3 months old.

Product Description

Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.

Distribution Pattern

Domestic: AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MN, MO, MS, NC, NJ, NY, OH, OK, OR, TN, TX, VT, WA, WI, WV, WY. International: Australia, Belgium, Brazil, France, Germany, Portugal, UK

Other Recalls by FUJIFILM Healthcare Americas Corporation

• Class II: Risk 01/09/2026
  It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be supplied to the power supply circuit even if the power of the device is cut off. As a result, it cannot be denied that the circuit in question overheats and damages the surrounding parts. It may also cause smoke.
• Class II: Risk 09/15/2025
  It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
• Class II: Risk 06/11/2025
  Devices had an unapproved slabbing software function enabled for use.

View all recalls by FUJIFILM Healthcare Americas Corporation →