Alcon Research, LTD. FDA Recalls

6 recalls on file across devices, 0 of them Class I and 6 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Legion FMS PakClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023
Constellation Procedure PakClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023
Infinity FMS PakClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023
Alcon Custom PakClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023
Centurion FMS PakClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023
Phaco Standalone TipsClass IIJun 28, 2023Reports of patient injury during use in procedures due to po	Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening wi	Class IIDevices	Jun 28, 2023