MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2005-11-03 for BASIC VENTURI PHACO PACK DP4305E manufactured by Bausch & Lomb, Inc..
[405735]
Aspiration problems during the procedure resulted in the need to perform an extracapsular procedure. A stitch was required to close the wound. There was no additional pt injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1920664-2005-00113 |
MDR Report Key | 644306 |
Report Source | 05,07 |
Date Received | 2005-11-03 |
Date of Report | 2005-10-03 |
Date of Event | 2005-09-28 |
Date Mfgr Received | 2005-10-03 |
Device Manufacturer Date | 2005-06-01 |
Date Added to Maude | 2005-11-04 |
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 | 3 |
Event Location | 0 |
Manufacturer Contact | JACKIE FLACH |
Manufacturer Street | 3365 TREE COURT IND. BLVD. |
Manufacturer City | ST. LOUIS MO 63122 |
Manufacturer Country | US |
Manufacturer Postal | 63122 |
Manufacturer Phone | 6362263255 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BASIC VENTURI PHACO PACK |
Generic Name | OPTHTHALMIC MICROSURGICAL ACCESSORY PACK |
Product Code | MSR |
Date Received | 2005-11-03 |
Model Number | NA |
Catalog Number | DP4305E |
Lot Number | T5662 |
ID Number | NA |
Device Expiration Date | 2007-05-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 633794 |
Manufacturer | BAUSCH & LOMB, INC. |
Manufacturer Address | * ROCHESTER NY 14609 US |
Baseline Brand Name | BASIC VENTURI PHACO PACK |
Baseline Generic Name | OPHTHALMIC MICROSURGICAL ACCESSORY PACK |
Baseline Model No | NA |
Baseline Catalog No | DP4305E |
Baseline ID | NA |
Baseline Device Family | NA |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K980100 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2005-11-03 |