Trans American Medical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0532-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Spectre Wireless Footswitch/Handswitch system Model 98/99, Model FDS, Model FDB. The Spectre Wireless Encrypted Footswitch/Hand Switch System is a prescription use system and intended only for use with the system indicated in the model number

Product Classification:

Class II

Date Initiated: August 22, 2013

Date Posted: January 15, 2014

Recall Number: Z-0532-2014

Event ID: 66064

Reason for Recall:

TransAmerican Medical Imaging is recalling certain lots of TMI Spectre Wireless Footswitch/Hand switch for GE OEC 9800/9900 and Philips FDS and FDB Cath Labs due to potential safety issue related to the use of this product producing uncommanded X-ray.

Status: Terminated

Product Quantity: 68

Code Information:

Serial numbers NS 10324 through NS 10392

Distribution Pattern:

US Distribution: including states of: WA and UT.

Voluntary or Mandated:

Voluntary: Firm initiated