Trans American Medical, Inc. Recalls

Overview of recall records associated with Trans American Medical, Inc., including dates, categories and classifications where available.

1recall records

Jan 15, 2014latest record date

Jan 15, 2014earliest record date

Recall history in this database

Classification mix: Class II: 1.

Medical DeviceJan 15, 2014

Trans American Medical Spectre Wireless Footswitch/Handswitch system Model 98/99, Model FDS recall — FDA Z-0532-2014

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…

Class IIFDA: TerminatedTrans American Medical, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Trans American Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.