MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 2000-06-02 for JAY SEATING ADJUSTABLE SOLID SEAT NA manufactured by Sunrise Medical Mpd.
[191673]
Reporter claims the drop seat cracked while the chair was in use. No injuries reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1720745-2000-00006 |
MDR Report Key | 280290 |
Report Source | 00 |
Date Received | 2000-06-02 |
Date of Report | 2000-06-01 |
Date of Event | 2000-05-11 |
Date Mfgr Received | 2000-05-11 |
Date Added to Maude | 2000-06-06 |
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 | SERVICE PERSONNEL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | WENDY CAVANAUGH |
Manufacturer Street | 2842 BUSINESS PARK AVE |
Manufacturer City | FRESNO CA 93727 |
Manufacturer Country | US |
Manufacturer Postal | 93727 |
Manufacturer Phone | 5592922171 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | JAY SEATING |
Generic Name | WHEELCHAIR, ACCESSORY |
Product Code | KNO |
Date Received | 2000-06-02 |
Model Number | ADJUSTABLE SOLID SEAT |
Catalog Number | NA |
Lot Number | P/N 270 |
ID Number | NA |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 271250 |
Manufacturer | SUNRISE MEDICAL MPD |
Manufacturer Address | 7477 EAST DRY CREEK PKWY. LONGMONT CO 80503 US |
Baseline Brand Name | JAY SEATING |
Baseline Generic Name | WHEELCHAIR ACCESSORY |
Baseline Model No | ADJUSTABLE SOLI |
Baseline Catalog No | NA |
Baseline ID | NA |
Baseline Device Family | SEATING/POSITIONING SYSTEMS |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K901634 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2000-06-02 |