MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-08 for BENCHMARK ULTRA 750-600 05342716001 manufactured by Ventana Medical Systems.
[132570273]
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Patient Sequence No: 1, Text Type: N, H10
[132570274]
Instrument malfunction: tub overflow occurred and allowed fluid to reach floor. Tub sensor(s) did not properly report error and prevent fluid leak. The following failure mode is same event reported in mdr-2028492-2016-00004-00 which caused serious slip and fall injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2028492-2019-00001 |
MDR Report Key | 8229488 |
Date Received | 2019-01-08 |
Date of Report | 2019-01-08 |
Date of Event | 2018-12-10 |
Date Mfgr Received | 2018-12-10 |
Date Added to Maude | 2019-01-08 |
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 | 3 |
Event Location | 3 |
Manufacturer Contact | NA TIM GIBLIN |
Manufacturer Street | 1910 EAST INNOVATION PARK DR NA |
Manufacturer City | TUSCON AZ 85755 |
Manufacturer Country | US |
Manufacturer Postal | 85755 |
Manufacturer Phone | 5208777035 |
Single Use | 3 |
Remedial Action | RP |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 0 |
Brand Name | BENCHMARK ULTRA |
Generic Name | BENCHMARK ULTRA |
Product Code | PPM |
Date Received | 2019-01-08 |
Model Number | 750-600 |
Catalog Number | 05342716001 |
Lot Number | 311423 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VENTANA MEDICAL SYSTEMS |
Manufacturer Address | 1910 E. INNOVATION PARK DR. NA TUCSON AZ 857551962 US 857551962 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-01-08 |