MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,user facility report with the FDA on 2019-01-11 for 6715 KERLIX RL STERILE 1'S manufactured by Covidien.
[132844371]
The incident sample has been requested but to date has not been received for evaluation. If the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted. As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
Patient Sequence No: 1, Text Type: N, H10
[132844372]
Customer reports that the xray detectable string came unattached from the kerlix sponge.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1018120-2019-00327 |
MDR Report Key | 8241251 |
Report Source | DISTRIBUTOR,USER FACILITY |
Date Received | 2019-01-11 |
Date of Report | 2019-02-13 |
Date of Event | 2019-01-07 |
Date Mfgr Received | 2019-01-07 |
Date Added to Maude | 2019-01-11 |
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 | JILL SARAIVA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5084524970 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | 1430 MARVIN GRIFFIN ROAD, PO B |
Manufacturer City | AUGUSTA GA 30906 |
Manufacturer Country | US |
Manufacturer Postal Code | 30906 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 6715 KERLIX RL STERILE 1'S |
Generic Name | GAUZE/SPONGE,NONRESORBABLE FOR EXTERNAL USE |
Product Code | NAB |
Date Received | 2019-01-11 |
Model Number | 6715 |
Catalog Number | 6715 |
Lot Number | 18D018962 |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 1430 MARVIN GRIFFIN ROAD, PO B AUGUSTA GA 30906 US 30906 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-01-11 |