MAUDE Adverse Event Report: STAAR SURGICAL COMPANY ICL (IMPLANTABLE COLLAMER LENS); INTRAOCULAR LENS

Model Number	MICL12.6
Medical Device Problem Code	Inadequacy of Device Shape and/or Size (1583)
Health Effect - Clinical Codes	Glaucoma (1875); Intraocular Pressure Increased (1937); No Code Available (3191)
Date of Event	10/10/2016
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Lens not returned.
Event or Problem Description
The reporter stated that the surgeon implanted a 12.6mm micl12.6 lens, -3.50 diopter, in the patient's right eye on (b)(6) 2016.Following the surgery, the patient experienced narrowing of the angle and shallowing of the acd.On (b)(6) 2016, the patient had elevated intraocular pressure (iop) and closed angle glaucoma due to excessive vaulting of the lens.The patient received a yag peripheral iridotomy, and the lens was explanted.The lens was exchanged for a shorter lens.
Additional Manufacturer Narrative
Device evaluation: product evaluation found that the lens was returned in liquid in the lens vial with clear surgical residue on the lens.Visual inspection found no visible damage to the lens.(b)(4).

• Brand Name: ICL (IMPLANTABLE COLLAMER LENS)
• Common Device Name: INTRAOCULAR LENS
• Manufacturer (Section D): STAAR SURGICAL COMPANY; 1911 walker avenue; monrovia CA 91016
• MDR Report Key: 6054107
• Report Number: 2023826-2016-01522
• Device Sequence Number: 11003463
• Product Code: MTA
• UDI-Device Identifier: 00841542102896
• UDI-Public: (01)00841542102896(17)171031
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: P030016
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: user facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/10/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Physician
• Device Expiration Date: 10/31/2017
• Device Model Number: MICL12.6
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/29/2016
• Type of Report(Section G): FDA Requested
• Initial Date Received by Manufacturer: 10/10/2016
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 10/25/2016
• Supplement Report FDA Received Date: 12/02/2016
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CARTRIDGE MODEL UNK, LOT NUMBER UNK; INJECTOR MODEL UNK, LOT NUMBER UNK
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 30 YR