MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2012-06-08 for ACCURUS 400 VS 8065740238 manufactured by Alcon - Irvine Technology Center.
[2765530]
A customer reported that the equipment displayed deficient aspiration and fluid/gas exchange failure during a vitrectomy procedure. After a delay of more than 15 minutes, the case was able to be completed with the same equipment. Add'l info has been requested.
Patient Sequence No: 1, Text Type: D, B5
[9920761]
Investigation including root cause analysis, is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when add'l reportable info becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2028159-2012-00838 |
MDR Report Key | 2617337 |
Report Source | 01,05 |
Date Received | 2012-06-08 |
Date of Report | 2012-05-10 |
Date of Event | 2012-04-26 |
Date Mfgr Received | 2012-05-10 |
Device Manufacturer Date | 2008-05-01 |
Date Added to Maude | 2012-09-12 |
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 | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | PAUL NITSCHMANN |
Manufacturer Street | 6201 SOUTH FREEWAY, R3-16 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152440 |
Manufacturer G1 | ALCON - IRVINE TECHNOLOGY CENTER |
Manufacturer Street | 15800 ALTON PKWY. |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ACCURUS 400 VS |
Generic Name | PHACOFRAGMENTATION SYSTEM |
Product Code | HLM |
Date Received | 2012-06-08 |
Model Number | ACCURUS |
Catalog Number | 8065740238 |
Lot Number | NA |
ID Number | 4.54 |
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 CENTER |
Manufacturer Address | 15800 ALTON PKWY. IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-06-08 |