Atlas FDA

ConMed Linvatec MicroChoice Footswitch and ConMed linvatec 3 Pedal Footswitch. Used to operate various surgical handpiec

FDA device recall Z-1444-06 · posted 2006-08-29 · Terminated

Recall details

Recalling firm
Linvatec Corp.
Reason for recall
The footswitch may develop a system fault resulting in the self-activation of the handpiece it controls, or it may cause the handpiece to run intermittently or to revert to a default setting.
Action taken
Linvatec has issued recall notification to all it''s direct accounts. The mailings were sent by UPS 08/31/2005. Each consignee was requested to return the affected product to Linvatec for a free replacement footswitch.
Root cause
Other
Status
Terminated
Product code
GEY
Quantity affected
118
Distribution
Worldwide, including United States and Canada.
Date initiated
2005-08-30
Date posted
2006-08-29
Date terminated
2012-07-13
Location
Largo, FL

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.