MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,07 report with the FDA on 2015-07-29 for DEK BL MF 0 TC-43/HR 26 2N 833-124 manufactured by Teleflex Medical.
[6634443]
Alleged event: the suture broke during bending. The patient's condition was reported as recovering.
Patient Sequence No: 1, Text Type: D, B5
[14306285]
(b)(4). The device history of batch number (b)(4) has been reviewed and no issues or discrepancies were found which could potentially relate to this complaint. The manufacturer will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3004365956-2015-00197 |
| MDR Report Key | 4950516 |
| Report Source | 01,05,07 |
| Date Received | 2015-07-29 |
| Date of Report | 2015-07-14 |
| Date of Event | 2015-07-03 |
| Date Mfgr Received | 2015-07-14 |
| Device Manufacturer Date | 2015-01-05 |
| Date Added to Maude | 2015-07-29 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | EFFIE JEFFERSON |
| Manufacturer Street | 3015 CARRINGTON MILL BLVD |
| Manufacturer City | MORRISVILLE NC 27560 |
| Manufacturer Country | US |
| Manufacturer Postal | 27560 |
| Manufacturer Phone | 9194332672 |
| Manufacturer G1 | TELEFLEX MEDICAL |
| Manufacturer Street | PARQUE INDUSTRIAL FINSA |
| Manufacturer City | NUEVO LAREDO 88275 |
| Manufacturer Country | MX |
| Manufacturer Postal Code | 88275 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DEK BL MF 0 TC-43/HR 26 2N |
| Generic Name | SUTURE |
| Product Code | OVN |
| Date Received | 2015-07-29 |
| Catalog Number | 833-124 |
| Lot Number | 74A1501230 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL |
| Manufacturer Address | RESEARCH TRIANGLE PARK NC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2015-07-29 |