MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-06-28 for LMA GASTRO CUFF PILOT SIZE 4 1E5040 manufactured by Teleflex Medical.
[149647110]
Qn# (b)(4). The patient's condition was critical but this was not related to the lma. The lma was removed following difficulty of passing through the scope. No injury noted as a result of the scope not passing through the lma nor was any injury noted following removal of the lma. The procedure proceeded without the lma.
Patient Sequence No: 1, Text Type: N, H10
[149647111]
It was reported that "the endoscopist raised concerns that he found it difficult to pass the scope through the lma". No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9681900-2019-00022 |
| MDR Report Key | 8745213 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-06-28 |
| Date of Report | 2019-06-28 |
| Date of Event | 2019-04-12 |
| Date Mfgr Received | 2019-08-01 |
| Date Added to Maude | 2019-06-28 |
| 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 GASTRO CUFF PILOT SIZE 4 |
| Generic Name | LMA GASTRO CUFF PILOT |
| Product Code | CAE |
| Date Received | 2019-06-28 |
| Catalog Number | 1E5040 |
| Lot Number | MMCDXP |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| 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 | 2019-06-28 |