MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-29 for DERMACEA 441601 manufactured by Covidien.
[93457897]
Submit date: 11/14/2017. An investigation is currently under way; upon completion the results will be forwarded. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[93457898]
The customer reported that the sponges were severely linting.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3008361498-2017-05564 |
MDR Report Key | 7068592 |
Date Received | 2017-11-29 |
Date of Report | 2018-02-27 |
Date Mfgr Received | 2017-11-03 |
Date Added to Maude | 2017-11-29 |
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 | EDWARD ALMEIDA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5084524151 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | 15 HAMPSHIRE ST. |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal Code | 02048 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | DERMACEA |
Generic Name | GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE |
Product Code | NAB |
Date Received | 2017-11-29 |
Model Number | 441601 |
Catalog Number | 441601 |
Lot Number | 17063008 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 15 HAMPSHIRE ST. MANSFIELD MA 02048 US 02048 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-11-29 |