MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01 report with the FDA on 2014-05-20 for ACCURUS HIGH BRIGHTNESS ILLUMINATOR SYSTEM 8065750290 manufactured by Alcon -irvine Technology Ctr.
[20718358]
A customer reported the system shut down on its own, during a vitrectomy procedure. The case was completed after rebooting the system. There was no harm to the pt.
Patient Sequence No: 1, Text Type: D, B5
[21002065]
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 info becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2028159-2014-00957 |
MDR Report Key | 3876097 |
Report Source | 00,01 |
Date Received | 2014-05-20 |
Date of Report | 2014-04-25 |
Date of Event | 2014-04-25 |
Date Mfgr Received | 2014-04-25 |
Device Manufacturer Date | 2011-01-01 |
Date Added to Maude | 2014-06-30 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JANET MORAN |
Manufacturer Street | 6201 S FREEWAY R3-48 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152742 |
Manufacturer G1 | ALCON -IRVINE TECHNOLOGY CTR |
Manufacturer Street | 15800 ALTON PKWY. |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ACCURUS HIGH BRIGHTNESS ILLUMINATOR SYSTEM |
Generic Name | ENDOILLUMINATOR |
Product Code | MPA |
Date Received | 2014-05-20 |
Model Number | NA |
Catalog Number | 8065750290 |
Lot Number | NA |
ID Number | 1.18 - 2.18 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON -IRVINE TECHNOLOGY CTR |
Manufacturer Address | 15800 ALTON PKWY. IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-05-20 |