GRIESHABER DSP SURGICAL CONTACT LENS
Report
- Report Number
- 3003398873-2023-00127
- Event Type
- Injury
- Date Received
- June 26, 2023
- Date of Event
- May 1, 2023
- Report Date
- September 13, 2023
- Manufacturer
- ALCON GRIESHABER AG
- Product Code
- HJI
- UDI-DI
- 07612717071285
- PMA / PMN Number
- EXEMPT
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
INVESTIGATION INCLUDING ROOT CAUSE ANALYSIS IS IN PROGRESS. A SUPPLEMENTAL MDR WILL BE FILED AS NECESSARY IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL REPORTABLE INFORMATION BECOMES AVAILABLE. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).
NO LOT NUMBER WAS IDENTIFIED AND THEREFORE WITHIN THIS COMPLAINT, THE ASSOCIATED MANUFACTURING DOCUMENTATION COULD NOT BE REVIEWED. ALL PRODUCT AND BATCH HISTORY RECORDS ARE QUALITY REVIEWED PRIOR TO PRODUCT RELEASE, ENSURING THAT ALL PRODUCTS ON THE MARKET FULFILL THE RELEVANT REQUIREMENTS. NO SAMPLE IS AVAILABLE TO BE PROVIDED TO THE RESPONSIBLE SITE FOR AN IN-DEPTH INVESTIGATION. NOT ENOUGH INFORMATION WAS PROVIDED TO PROPERLY COMPLETE AN INVESTIGATION. THE ROOT CAUSE OF THIS COMPLAINT COULD NOT BE IDENTIFIED. THE EXACT ROOT CAUSE FOR THE CUSTOMER¿S REPORTED EVENT IS UNKNOWN. THEREFORE, NO SPECIFIC ACTION CAN BE TAKEN. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).
A CLINICAL STUDY REVEALED THAT DURING THE MEMBRANE PEELING SURGERY WHILE USING DISPOSABLE LENS A MALE PATIENT EXPERIENCED OCULAR TOXICITY (MACULAR) RESPONSE. PATIENT SYMPTOM'S WAS RESOLVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1542067 | GRIESHABER DSP SURGICAL CONTACT LENS | LENS, FUNDUS, HRUBY, DIAGNOSTIC | HJI | ALCON GRIESHABER AG | NA | ASKU | 07612717071285 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Male | Other | VOLK SINGLE USE LENSES |