MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2012-12-19 for TRANSFER CART manufactured by Steris Canada Corporation.
[3528678]
The user facility reported that the employee is back to normal work duties.
Patient Sequence No: 1, Text Type: D, B5
[16916710]
The user facility reported that an employee injured his back while attempting to prevent the cart from tipping over. The employee went to a clinic where he was examined and given an anti inflammatory injection and prescribed medication. No procedural delays or cancellations reported.
Patient Sequence No: 1, Text Type: D, B5
[17086266]
A steris service technician inspected the transfer cart and found a wheel had detached. The technician stated that the wheel coming off can be attributed to a nut in the wheel coming loose. The technician reinstalled the wheel and secured it, checked the additional wheels and confirmed it to be operational. The transfer cart is not under steris service contract and is serviced and maintained by the user facility.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 9680353-2012-00126 |
| MDR Report Key | 2880223 |
| Report Source | 06 |
| Date Received | 2012-12-19 |
| Date of Report | 2012-12-19 |
| Date of Event | 2012-12-04 |
| Date Mfgr Received | 2012-12-04 |
| Date Added to Maude | 2013-03-22 |
| 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 | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MS LINDSEY MCGOWAN |
| Manufacturer Street | 5960 HEISLEY ROAD |
| Manufacturer City | MENTOR OH 44060 |
| Manufacturer Country | US |
| Manufacturer Postal | 44060 |
| Manufacturer Phone | 4403927519 |
| Manufacturer G1 | STERIS CANADA CORPORATION |
| Manufacturer Street | 490, ARMAND-PARIS |
| Manufacturer City | QUEBEC, QUEBEC GIC8A3 |
| Manufacturer Country | CA |
| Manufacturer Postal Code | GIC 8A3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TRANSFER CART |
| Generic Name | TRANSFER CART |
| Product Code | LDS |
| Date Received | 2012-12-19 |
| Operator | OTHER HEALTH CARE PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STERIS CANADA CORPORATION |
| Manufacturer Address | 490 ARMAND-PARIS QUEBEC, QUEBEC GIC8A3 CA GIC 8A3 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-12-19 |