COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE
Report
- Report Number
- 2023826-2006-00815
- Event Type
- Malfunction
- Date Received
- June 23, 2006
- Date of Event
- May 25, 2006
- Report Date
- May 25, 2006
- Manufacturer
- STAAR SURGICAL CO.
- Product Code
- HQL
- PMA / PMN Number
- p990013
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
Narratives
H6: EVALUATION RESULTS - VISUAL INSPECTION OF THE RETURNED PRODUCT FOUND THE LENS OPTIC TORN. THERE WAS EVIDENCE OF CLEAR SURGICAL RESIDUE. A LENS WORK ORDER SEARCH WAS PERFORMED AND NO SIMILAR COMPLAINTS WERE FOUND WITHIN THE WORK ORDER. A CARTRIDGE WORK ORDER SEARCH WAS PERFORMED AND TWO SIMILAR COMPLAINTS WERE FOUND WITHIN THE LOT OF PRODUCT. CONCLUSIONS - (NO CONCLUSION CAN BE DRAWN): BASED ON THE COMPLAINT HISTORY, THE WORK ORDER SEARCHES AND THE EVALUATION OF THE RETURNED PRODUCT, A SPECIFIC ROOT CAUSE OF THE EVENT COULD NOT BE DETERMINED. IT SHOULD BE NOTED THAT THE INJECTOR AND CARTRIDGE WERE NOT RETURNED FOR EVALUATION. PMA# P990013.
IT WAS REPORTED THAT THE SURGEON ATTEMPTED TO INSERT A CQ2015 COLLAMER THREE-PIECE LENS. BUT THOUGHT HE SAW A TEAR, SO EJECTED THE LENS ONTO THE STERILE FIELD. THERE WAS A TEAR AT BOTH HAPTIC JUNCTIONS. THERE WAS NO PATIENT CONTACT. THIS IS ONE OF TWO LENSES USED ON THIS PATIENT - SEE MFR. REPORT# 2023826-2006-00813.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE | INTRAOCULAR LENS | HQL | STAAR SURGICAL CO. | CQ2015 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR | INJECTOR MODEL MSI-PM - LOT NUMBER UNK| CARTRIDGE MODEL CQ CARTRIDGE-FP - LOT # 1212554 |