MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 1998-07-14 for 7688 L A NA manufactured by Crow River Industries, Inc..
        [120917]
Report of alleged "pt injured while using a crow river lift. " source had one of their employees injured while unfolding the platform.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2183897-1998-00003 | 
| MDR Report Key | 177771 | 
| Report Source | 08 | 
| Date Received | 1998-07-14 | 
| Date of Report | 1998-07-14 | 
| Date of Event | 1998-07-02 | 
| Date Mfgr Received | 1998-07-02 | 
| Device Manufacturer Date | 1997-11-01 | 
| Date Added to Maude | 1998-07-21 | 
| 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 | 0 | 
| Single Use | 3 | 
| Remedial Action | OT | 
| Previous Use Code | 3 | 
| Removal Correction Number | NA | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | 7688 L A | 
| Generic Name | AUTOMATIC VAN LIFT | 
| Product Code | ING | 
| Date Received | 1998-07-14 | 
| Model Number | 7688 | 
| Catalog Number | NA | 
| Lot Number | NA | 
| ID Number | NA | 
| Operator | UNKNOWN | 
| Device Availability | N | 
| Device Age | 8 MO | 
| Device Eval'ed by Mfgr | R | 
| Implant Flag | N | 
| Date Removed | A | 
| Device Sequence No | 1 | 
| Device Event Key | 172857 | 
| Manufacturer | CROW RIVER INDUSTRIES, INC. | 
| Manufacturer Address | 850 STATE HIGHWAY 55 PO BOX 70 BROOTEN MN 56316 US | 
| Baseline Brand Name | MINI-VANGATER LIFT | 
| Baseline Generic Name | WHEELCHAIR LIFT | 
| Baseline Model No | 7688 | 
| Baseline Catalog No | NA | 
| Baseline ID | NA | 
| Baseline Device Family | AUTOMATIC VAN LIFT | 
| Baseline Shelf Life [Months] | NA | 
| Baseline PMA Flag | N | 
| Baseline 510K PMN | Y | 
| Premarket Notification | K900417 | 
| Baseline Preamendment | N | 
| Baseline Transitional | N | 
| 510k Exempt | N | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Other | 1998-07-14 |