Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Spectre Wireless Footswitch/Handswitch system Model 98/99 Recalled by Trans American Medical, Inc. Due to TransAmerican Medical Imaging is recalling certain lots of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Trans American Medical, Inc. directly.
Affected Products
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
Quantity: 68
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 2 states: UT, WA
About Trans American Medical, Inc.
Trans American Medical, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report