MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2018-12-21 for HELIOS H46T B-700847-00 manufactured by Caire Inc..
[131163483]
Unit is being returned for evaluation by manufacturer. If any new information is discovered, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[131163484]
The patient filled his portable h300 with the helios unit ; then he went to his kitchen and he heard some noise. He came back to see the helios unit and noticed that it was leaking ; trying to stop the leak, he burnt 3 fingers. The patient went to the emergency but didn't stay at the hospital. Now he has no more pain but said he missed a bit sensitivity.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3004972304-2018-00056 |
MDR Report Key | 8189351 |
Report Source | FOREIGN |
Date Received | 2018-12-21 |
Date of Report | 2018-12-21 |
Date of Event | 2018-11-08 |
Date Mfgr Received | 2018-11-22 |
Date Added to Maude | 2018-12-21 |
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. NEAL MALOY |
Manufacturer Street | 2200 AIRPORT INDUSTRIAL DRIVE SUITE 500 |
Manufacturer City | BALL GROUND GA 30107 |
Manufacturer Country | US |
Manufacturer Postal | 30107 |
Manufacturer G1 | CAIRE INC. |
Manufacturer Street | 2200 AIRPORT INDUSTRIAL DRIVE SUITE 500 |
Manufacturer City | BALL GROUND GA 30107 |
Manufacturer Country | US |
Manufacturer Postal Code | 30107 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HELIOS H46T |
Generic Name | UNIT, LIQUID OXYGEN, STATIONARY |
Product Code | BYJ |
Date Received | 2018-12-21 |
Returned To Mfg | 2019-01-08 |
Model Number | B-700847-00 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CAIRE INC. |
Manufacturer Address | 2200 AIRPORT INDUSTRIAL DRIVE SUITE 500 BALL GROUND GA 30107 US 30107 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2018-12-21 |