MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2006-10-11 for RETROGUARD ARTERIAL SAFETY VALVE 4007200 * manufactured by Quest Medical, Inc..
[471508]
The customer returned a valve and a note to a quest sales rep at the amsect show. The product was a retroguard, product code 4007200. The device had a crack. This is the only info provided to quest. Product code 4007200, lot 25304.
Patient Sequence No: 1, Text Type: D, B5
[7840551]
A crack was noticed on the housing: however, the device was tested and passed our pressure decay test that is performed during normal mfg. This concludes that the crack does not affect functionality nor will it cause any leaking. This complaint condition is considered to be a cosmetic defect.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1649914-2006-00046 |
| MDR Report Key | 717930 |
| Report Source | 06 |
| Date Received | 2006-10-11 |
| Date of Report | 2006-05-04 |
| Date of Event | 2006-04-04 |
| Date Mfgr Received | 2006-04-24 |
| Device Manufacturer Date | 2005-11-01 |
| 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 | MEGAN SIMS |
| 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 | RETROGUARD ARTERIAL SAFETY VALVE |
| Generic Name | FLOW CHECK VALVE |
| Product Code | MJJ |
| Date Received | 2006-10-11 |
| Returned To Mfg | 2006-04-24 |
| Model Number | 4007200 |
| Catalog Number | * |
| Lot Number | 25304 |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 707005 |
| Manufacturer | QUEST MEDICAL, INC. |
| Manufacturer Address | ONE ALLENTOWN PKWY. ALLEN TX 75002 US |
| Baseline Brand Name | RETROGUARD |
| Baseline Generic Name | FLOW CHECK VALVE |
| Baseline Model No | 4007200 |
| Baseline Catalog No | * |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-10-11 |