MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1998-02-24 for KAHN SCLERAL SHIELD ET4600 manufactured by Storz Instrument Co..
[93300]
The handle broke off of this scleral shield during a procedure. Another shield was used. There was no pt injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1932180-1998-00010 |
MDR Report Key | 151427 |
Report Source | 06 |
Date Received | 1998-02-24 |
Date of Report | 1998-01-27 |
Date of Event | 1998-01-22 |
Date Facility Aware | 1998-01-22 |
Report Date | 1998-01-27 |
Date Mfgr Received | 1998-01-22 |
Date Added to Maude | 1998-02-26 |
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 | KAHN SCLERAL SHIELD |
Generic Name | EYE SHIELD |
Product Code | HOY |
Date Received | 1998-02-24 |
Model Number | NA |
Catalog Number | ET4600 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | UNKNOWN |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 147571 |
Manufacturer | STORZ INSTRUMENT CO. |
Manufacturer Address | 499 SOVEREIGN CT. MANCHESTER MO 63011 US |
Baseline Brand Name | KAHN SCLERAL SHIELD |
Baseline Generic Name | OPHTHALMIC EYE SHIELD |
Baseline Model No | NA |
Baseline Catalog No | ET4600 |
Baseline ID | NA |
Baseline Device Family | EYE SHIELD |
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 | 1998-02-24 |