MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2006-05-16 for LACRICATH LACRIMAL DUCT CATHETER, 2.0MM LDC213 * manufactured by Quest Medical, Inc..
[19489708]
During a dcp procedure, the balloon catheter was in place and upon inflation, it was discovered that the catheter was leaking from the balloon end. Another catheter was used to complete the procedure without any complications. The complaint sample was saved and will be returned to quest for evaluation. The device is packaged in a kit. The pary number of the kit ldc213, the reported lot number is not for the reported code.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1649914-2006-00044 |
| MDR Report Key | 717906 |
| Report Source | 06 |
| Date Received | 2006-05-16 |
| Date of Report | 2006-05-04 |
| Date Mfgr Received | 2006-04-21 |
| Date Added to Maude | 2006-05-25 |
| 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 | 0 |
| Manufacturer Contact | KATHRYN JAYNE |
| Manufacturer Street | ONE ALLENTOWN PARKWAY |
| Manufacturer City | ALLEN TX 75002 |
| Manufacturer Country | US |
| Manufacturer Postal | 75002 |
| Manufacturer Phone | 9723909800 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LACRICATH LACRIMAL DUCT CATHETER, 2.0MM |
| Generic Name | MANUAL OPHTHALMIC SURGICAL INSTRUMENT: LACRYMAL DILATOR |
| Product Code | HNW |
| Date Received | 2006-05-16 |
| Returned To Mfg | 2006-04-26 |
| Model Number | LDC213 |
| Catalog Number | * |
| Lot Number | UNK |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | * |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 706974 |
| Manufacturer | QUEST MEDICAL, INC. |
| Manufacturer Address | ONE ALLENTOWN PKWY. ALLEN TX 75002 US |
| Baseline Brand Name | LACRICATH 2.0MM |
| Baseline Generic Name | LACRIMAL DUCT BALLOON CATHETER |
| Baseline Model No | LDC213 |
| Baseline Catalog No | * |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-05-16 |