MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-01-23 for CYLINDER CART 36265 00001 81-2000 manufactured by Anthony Welded Products.
[3239234]
We purchased 40 cylinder carts from tri-anim in (b)(6) 2012. I have 5 with the gurney hooks broken off or cracked at the bottom of the weld. We are checking them as we find them.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5028781 |
| MDR Report Key | 2935583 |
| Date Received | 2013-01-23 |
| Date of Report | 2013-01-23 |
| Date of Event | 2013-01-15 |
| Date Added to Maude | 2013-01-31 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CYLINDER CART |
| Generic Name | CYLINDER CART |
| Product Code | PCM |
| Date Received | 2013-01-23 |
| Model Number | 36265 00001 |
| Catalog Number | 81-2000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ANTHONY WELDED PRODUCTS |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-01-23 |