Coherent Inc Laser Group Coherent brand Quattro Diode Laser Systems; A Quattro FAP System; Model Numbers/Serial Numbers: TFAP0004P--TFAP00048 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Coherent brand Quattro Diode Laser Systems; A Quattro FAP System; Model Numbers/Serial Numbers: TFAP0004P--TFAP00048
Brand
Coherent Inc Laser Group
Lot Codes / Batch Numbers
Serial Numbers/Model Numbers: TFAP0004P--TFAP00048
Products Sold
Serial Numbers/Model Numbers: TFAP0004P--TFAP00048
Coherent Inc Laser Group is recalling Coherent brand Quattro Diode Laser Systems; A Quattro FAP System; Model Numbers/Serial Numbers: TF due to Software problem that may cause the instrument to remain on and emitting laser radiation after the interlock has been activated.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software problem that may cause the instrument to remain on and emitting laser radiation after the interlock has been activated.
Recommended Action
Per FDA guidance
On 11/7/03, all consignees were notified via Certified Mail and on-site visit by the firm''s sales representative, informing them of the affected devices and providing instructions on the recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026