MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-01-07 for ULTRATHANE MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER N/A ULT10.2-38-25-P-6S-CLM-RH manufactured by Cook Inc.
[188480783]
Initial reporter occupation: lead tech. Pma/510(k) #: exempt. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[188480784]
It was reported an ultrathane mac-loc locking loop multipurpose drainage catheter was used in an unknown patient for drainage. Two days after placement, the device stopped draining and was suspected to be kinked. The device was replaced with a new, similar device successfully. No other adverse effects were reported for this incident.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1820334-2020-00077 |
MDR Report Key | 9559969 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-01-07 |
Date of Report | 2020-01-13 |
Date of Event | 2020-01-06 |
Date Mfgr Received | 2020-03-03 |
Date Added to Maude | 2020-01-07 |
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 | MRS. JENNIFER CANADA |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal | 47404 |
Manufacturer Phone | 8123392235 |
Manufacturer G1 | COOK INC |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal Code | 47404 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ULTRATHANE MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER |
Generic Name | GBO CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY |
Product Code | GBO |
Date Received | 2020-01-07 |
Returned To Mfg | 2020-01-14 |
Model Number | N/A |
Catalog Number | ULT10.2-38-25-P-6S-CLM-RH |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK INC |
Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other; 2. Required No Informationntervention | 2020-01-07 |