MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1998-12-16 for LINDSTROM ASPIRATING SPECULUM E4067 manufactured by Bausch & Lomb Surgical.
[20930477]
This instrument broke during a procedure. There was no effect on the pt.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1932180-1998-00071 |
MDR Report Key | 202569 |
Report Source | 05,06 |
Date Received | 1998-12-16 |
Date of Report | 1998-11-16 |
Date of Event | 1998-11-13 |
Date Facility Aware | 1998-11-13 |
Report Date | 1998-11-16 |
Date Reported to Mfgr | 1998-11-16 |
Date Mfgr Received | 1998-11-16 |
Date Added to Maude | 1998-12-21 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LINDSTROM ASPIRATING SPECULUM |
Generic Name | NON-ILLUMINATED SPECULUM |
Product Code | HNC |
Date Received | 1998-12-16 |
Model Number | NA |
Catalog Number | E4067 |
Lot Number | NA |
ID Number | NA |
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 | 196767 |
Manufacturer | BAUSCH & LOMB SURGICAL |
Manufacturer Address | 499 SOVEREIGN COURT ST. LOUIS MO 63011 US |
Baseline Brand Name | LINDSTROM ASPIRATING SPECULUM |
Baseline Generic Name | SPECULUM |
Baseline Model No | NA |
Baseline Catalog No | E4067 |
Baseline ID | NA |
Baseline Device Family | SPECULUM |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1998-12-16 |