FDA Adverse Event Injury Summary report: N

IMPLANTABLE COLLAMER LENS (ICL)

MDR report key: 18602467 · Received January 29, 2024

Report

Report Number
2023826-2024-00189
Event Type
Injury
Date Received
January 29, 2024
Date of Event
January 1, 2024
Report Date
January 1, 2024
Manufacturer
STAAR SURGICAL COMPANY
Product Code
QCB
UDI-DI
00840311326754
PMA / PMN Number
P030016
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H6: HEALTH IMPACT - ADDITIONAL SURGERY: 4625 - AC WASHOUT. H6: HEALTH EFFECT IMPACT CODE- MEDICATION REQUIRED: 4644 - INTRACAMERAL MOXIFLOXACIN; PREDNISOLONE ACETATE; FORTIFIED VANCOMYCIN/TOBRAMYCIN; PRED-MOXI-BROM. H6 - WORK ORDER SEARCH: NO SIMILAR COMPLAINT WAS REPORTED FOR UNITS WITHIN THE SAME LOT. CLAIM#: (B)(4).

Description of Event or Problem · 0

THE REPORTER INDICATED THE SURGEON IMPLANTED A 13.2MM VTICMO13.2 IMPLANTABLE COLLAMER LENS -16.50/+1.00/076 (SPHERE/CYLINDER/AXIS) INTO THE PATIENT`S LEFT EYE (OS) ON (B)(6) 2023. ON (B)(6) 2024, INFLAMMATION WAS DIAGNOSED (EYE WAS RED AND PAINFUL). ADDITIONAL DIAGNOSTICS WERE PERFORMED SUCH AS MACULAR OCT AND VITREOUS CULTURES (NEGATIVE). SUBSEQUENT TREATMENTS WERE: AC WASHOUT, RETINA SURGEONS INJECTED ANTIBIOTICS. WITH PRESCRIPTION OF ADDITIONAL STEROIDS AND ANTIBIOTICS, BY ON (B)(6) 2024 ISSUES RESOLVED, THE EYE WAS WHITE AND QUIET, NEGATIVE SEIDEL TEST. ACCORDING TO THE SURGEON THE CAUSE OF THE EVENT WAS DUE TO A MEDICAL TRAUMA, DIFFICULT CASE; THE PUPIL WOULD NOT DILATE AND THE IRIS WAS MANIPULATED MORE THAN NORMAL. THE SURGEON INDICATES THIS WAS A CASE OF INFLAMMATION AND NOT INFECTION. THE LAST INFORMATION OBTAINED ON (B)(6) 2024 STATED THAT PATIENT CURRENT POST-OP PROTOCOL WAS PRED-MOXI-BROM TWICE A DAY. THE LENS REMAINS IMPLANTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1033133 IMPLANTABLE COLLAMER LENS (ICL) PHAKIC TORIC INTRAOCULAR LENS QCB STAAR SURGICAL COMPANY VTICMO13.2 NA 00840311326754

Patients

Seq Age Sex Outcome Treatment
1 31 YR Male Required Intervention UNK.