MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05,06 report with the FDA on 1997-10-29 for CHAIRMAN DENTAL CHAIR L1 007890 manufactured by Siemens Pelton & Crane.
[75434]
Pelton & crane received a call from a doctor's office regarding a second hand chairman dental chair that broke. The doctor said that he was reclining a patient in the chair when the chair's back assembly broke causing the patient to fall down. The doctor was not performing a procedure when the chair back broke. The doctor said that there were no visual signs of permanent or serious injuries to the patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1017522-1997-00125 |
MDR Report Key | 129529 |
Report Source | 04,05,06 |
Date Received | 1997-10-29 |
Date of Report | 1997-10-29 |
Date of Event | 1997-09-29 |
Date Mfgr Received | 1997-09-30 |
Device Manufacturer Date | 1977-05-01 |
Date Added to Maude | 1997-11-04 |
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 | 0 |
Reporter Occupation | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CHAIRMAN DENTAL CHAIR |
Generic Name | DENTAL OPERATORY CHAIR |
Product Code | KLC |
Date Received | 1997-10-29 |
Model Number | L1 |
Catalog Number | 007890 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 126691 |
Manufacturer | SIEMENS PELTON & CRANE |
Manufacturer Address | PO. BOX 7800 CHARLOTTE NC 282417800 US |
Baseline Brand Name | CHAIRMAN |
Baseline Generic Name | DENTAL CHAIR |
Baseline Model No | L1 |
Baseline Catalog No | 007890 |
Baseline ID | NA |
Baseline Device Family | DENTAL OPERATORY WITH ACCESSORIES |
Baseline Shelf Life Contained | A |
Baseline Shelf Life [Months] | * |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1997-10-29 |