MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,user faci report with the FDA on 2019-12-26 for LMA SUPREME SIZE 2.5 175025 manufactured by Teleflex Medical.
[182598137]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[182598138]
Customer complaint alleges the balloon did not inflate prior to patient use during functional testing. No patient involvement reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9681900-2019-00052 |
MDR Report Key | 9522141 |
Report Source | DISTRIBUTOR,FOREIGN,USER FACI |
Date Received | 2019-12-26 |
Date of Report | 2019-12-02 |
Date of Event | 2019-10-31 |
Date Mfgr Received | 2020-01-21 |
Date Added to Maude | 2019-12-26 |
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 | KATHARINE TARPLEY |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194334854 |
Manufacturer G1 | THE LARYNGEAL MASK COMPANY |
Manufacturer Street | 6 BATTERY ROAD #07-02 |
Manufacturer City | SINGAPORE 049909 |
Manufacturer Country | SN |
Manufacturer Postal Code | 049909 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LMA SUPREME SIZE 2.5 |
Generic Name | AIRWAY,OROPHARYNGEAL,ANESTHESIOLOGY |
Product Code | CAE |
Date Received | 2019-12-26 |
Catalog Number | 175025 |
Lot Number | PMBSBH |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | ATHLONE |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-26 |