Their is a potential that intraocular implant devices may not meet specifications.
Reason for recall: Their is a potential that intraocular implant devices may not meet specifications. Distribution: US: AR AZ CA CO CT FL GA HI ID IL IN KS KY LA MA MD MI MN MO MT NC ND NE NJ NV NY OH OK OR PA SC SD TN TX UT VA WA WI OUS: None Quantity: 3 units Lot/code info: Serial/UDI: T1366733/(01)00841542113809(11)230215(17)250131(21)T1366733; T1485721/(01)00841542113892(11)230503(17)250430(21)T1485721; T1347685/(01)00841542113700(11)230203(17)250131(21)T1347685
00841542113809, 00841542113892, 00841542113700
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.