MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-01 for IRIS URETERAL KIT 0220180518 manufactured by Stryker Endoscopy-san Jose.
[129048696]
The product was not returned for investigation therefore the reported failure mode was not confirmed. The failure mode will be monitored for future reoccurrence. Alleged failure: following surgery the patient reported pain in the abdomen. Probable root cause: printed markings missing, inconsistently spaced, or otherwise incorrect. Incorrect device dimensions. User confusion. The device manufacturer date is not known.
Patient Sequence No: 1, Text Type: N, H10
[129048697]
It was reported that the patient had pain in the abdomen.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0002936485-2018-00708 |
MDR Report Key | 8121874 |
Date Received | 2018-12-01 |
Date of Report | 2018-12-21 |
Date of Event | 2018-09-03 |
Date Mfgr Received | 2018-11-02 |
Date Added to Maude | 2018-12-01 |
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 | MR. CHESTER REBUGIO |
Manufacturer Street | 5900 OPTICAL COURT |
Manufacturer City | SAN JOSE CA 95138 |
Manufacturer Country | US |
Manufacturer Postal | 95138 |
Manufacturer Phone | 4087542000 |
Manufacturer G1 | STRYKER ENDOSCOPY-SAN JOSE |
Manufacturer Street | 5900 OPTICAL COURT |
Manufacturer City | SAN JOSE CA 95138 |
Manufacturer Country | US |
Manufacturer Postal Code | 95138 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | IRIS URETERAL KIT |
Generic Name | LIGHT, CATHETER, FIBEROPTIC, GLASS, URETERAL |
Product Code | FCS |
Date Received | 2018-12-01 |
Catalog Number | 0220180518 |
Lot Number | 2250826 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER ENDOSCOPY-SAN JOSE |
Manufacturer Address | 5900 OPTICAL COURT SAN JOSE CA 95138 US 95138 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-12-01 |