MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2012-02-14 for HUT EXT DR FINAL ASSY-STANDARD 404008 manufactured by Liebel-flarsheim Co..
[19874624]
On (b)(6): customer reports via phone that staff were performing a lithotripsy, stent removal and stent placement on an approximately (b)(6), under general anesthesia, when fluoro failed. Staff moved the patient onto another table and completed the procedure using a portable c-arm fluoro unit. Patient is fine. No reported injury.
Patient Sequence No: 1, Text Type: D, B5
[20277072]
Product monitoring follow up: hospital staff stated they had used a large amount of sheets to absorb fluid under the urology table and hit the splash crash guard micro switches. Once the staff removed all the sheets from under the table, reset the splash crash guard switches, and rebooted the system, all urology table functions returned and they have experienced no further issues with the urology table.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1518293-2012-00030 |
MDR Report Key | 2462723 |
Report Source | 05,06,07 |
Date Received | 2012-02-14 |
Date of Report | 2012-02-14 |
Date of Event | 2012-01-25 |
Date Mfgr Received | 2012-01-25 |
Device Manufacturer Date | 2010-01-01 |
Date Added to Maude | 2012-08-16 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | DAVID BENSON |
Manufacturer Street | 2111 EAST GALBRAITH RD. |
Manufacturer City | CINCINNATI OH 45237 |
Manufacturer Country | US |
Manufacturer Postal | 45237 |
Manufacturer Phone | 5139485719 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUT EXT DR FINAL ASSY-STANDARD |
Product Code | KQS |
Date Received | 2012-02-14 |
Model Number | HUT EXT DR |
Catalog Number | 404008 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | LIEBEL-FLARSHEIM CO. |
Manufacturer Address | 2111 EAST GALBRAITH RD. CINCINNATI OH 45237 US 45237 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-02-14 |