MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-02 for SHILEY 125137 manufactured by Mallinckrodt Medical.
[115925094]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[115925095]
According to the reporter, the device's tubing was missing in box. Customer indicated that there was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8020889-2018-00075 |
MDR Report Key | 7742268 |
Date Received | 2018-08-02 |
Date of Report | 2018-10-03 |
Date of Event | 2018-06-22 |
Date Mfgr Received | 2018-08-08 |
Device Manufacturer Date | 2017-10-18 |
Date Added to Maude | 2018-08-02 |
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 | AVI KLUGER |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 3035306582 |
Manufacturer G1 | MALLINCKRODT MEDICAL |
Manufacturer Street | CORNAMADDY |
Manufacturer City | ATHLONE 3810 |
Manufacturer Postal Code | 3810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | SHILEY |
Generic Name | ATTACHMENT, BREATHING, POSITIVE END EXPIRATORY PRESSURE |
Product Code | BYE |
Date Received | 2018-08-02 |
Model Number | 125137 |
Catalog Number | 125137 |
Lot Number | 201709355X |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MALLINCKRODT MEDICAL |
Manufacturer Address | CORNAMADDY ATHLONE 3810 3810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-08-02 |