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COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE Adverse Event — Malfunction (MDR 2023826-2008-00233)

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE Adverse Event — Malfunction (MDR 2023826-2008-00233) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE; Generic name: INTRAOCULAR LENS; Manuf

DeviceCOLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE
Generic nameINTRAOCULAR LENS
ManufacturerSTAAR SURGICAL CO.
Report number2023826-2008-00233
Event typeMalfunction
Product problemY
Date received2008-02-21
Report sourceHealth Professional, Company representation
NarrativeTHE REPORTER STATED, THE HAPTIC OF A CQ2015 COLLAMER THREE PIECE LENS WAS TORN. ADD'L INFO HAS BEEN REQUESTED BUT NONE HAS BEEN FORTHCOMING. IF ADD'L INFO BECOMES AVAILABLE, A SUPPLEMENTAL MEDWATCH WILL BE SENT.
SourceopenFDA MAUDE (device adverse events)

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