MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-30 for ENDOWRIST 470309 manufactured by Intuitive Surgical, Inc..
[185503045]
Broke with 3 lives left, wheel fell off back of instrument. Manufacturer response for mega suture cut needle, mega suture cut needle driver (per site reporter). Failure analysis investigations replicated/confirmed the customer reported defective i&a "wheel fell off the back of the instrument. " the instrument was found to hav an input disk broken. Input disk #7 was found completely detached from the base of the housing. Improper cleaning during reprocessing most commonly causes this failure.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9897179 |
MDR Report Key | 9897179 |
Date Received | 2020-03-30 |
Date of Report | 2020-03-02 |
Date of Event | 2020-01-10 |
Report Date | 2020-03-02 |
Date Reported to FDA | 2020-03-02 |
Date Reported to Mfgr | 2020-03-30 |
Date Added to Maude | 2020-03-30 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
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 | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ENDOWRIST |
Generic Name | SYSTEM,SURGICAL,COMPUTER CONTROLLED INSTRUMENT |
Product Code | NAY |
Date Received | 2020-03-30 |
Returned To Mfg | 2020-01-27 |
Model Number | 470309 |
Lot Number | N10190909(0139) |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | 1 DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTUITIVE SURGICAL, INC. |
Manufacturer Address | 1266 KIFER ROAD SUNNYVALE CA 94086 US 94086 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |