MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-03-27 for MMG H2O 8FR 100/BX 20096080 manufactured by Teleflex Medical Sdn. Bhd..
[186333798]
(b)(4). There were 5 boxes with 100 items in each box. The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10
[186333799]
It was reported that the insertion tray inside this kit is expired by 3 years. These were found upon receipt at a distributor's warehouse; they never reached a medical facility.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8040412-2020-00104 |
MDR Report Key | 9889198 |
Report Source | DISTRIBUTOR |
Date Received | 2020-03-27 |
Date of Report | 2020-03-05 |
Date of Event | 2020-03-05 |
Date Mfgr Received | 2020-03-05 |
Date Added to Maude | 2020-03-27 |
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 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | EFFIE JEFFERSON |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194332672 |
Manufacturer G1 | TELEFLEX MEDICAL SDN. BHD. |
Manufacturer Street | LOT NO : PT2577 JALEN PERUSAHAAN 4 KAMUNTING INDUSTRIAL ESTATE |
Manufacturer City | PERAK, WEST MALAYSIA 34600 |
Manufacturer Country | MY |
Manufacturer Postal Code | 34600 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MMG H2O 8FR 100/BX |
Generic Name | CATHETER, UROLOGICAL |
Product Code | GBM |
Date Received | 2020-03-27 |
Catalog Number | 20096080 |
Lot Number | 17FE24 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL SDN. BHD. |
Manufacturer Address | PERAK, WEST MALAYSIA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-27 |