Siemens Medical Solutions USA, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1136-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge

Product Classification:

Class II

Date Initiated: January 16, 2023

Date Posted: February 22, 2023

Recall Number: Z-1136-2023

Event ID: 91518

Reason for Recall:

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Status: Ongoing

Product Quantity: 4 units

Code Information:

a) 450: UDI/DI 405686923807410106, Material Number 10749669, Serial Number 10106; b) 600: UDI/DI 405686922450311120, Material Number 10749670, Serial Number 11120; UDI/DI 405686922450311116, Material Number 10749670, Serial Number 11116; c) 600 Edge: UDI/DI 405686918321311068, Material Number 10749672, Serial Number 11068

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Japan, Chile, Australia.

Voluntary or Mandated:

Voluntary: Firm initiated