MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-04-07 for BARD DISPOZ-A-BAG LEG BAG UNK manufactured by Productos Para El Cuidado De La Salud -9611590.
[72411303]
The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard.
Patient Sequence No: 1, Text Type: N, H10
[72411304]
It was reported that urine leaked into the inlet tube. Subsequently, urine would not flow into the tube.
Patient Sequence No: 1, Text Type: D, B5
[79163899]
Received 1 used dizpoz-a-bag only. The reported event was unconfirmed, as the problem could not be reproduced. The visual inspection noted no obvious defects on the sample received. The sample was inspected and did not see any folds in the flutter valve that could have contributed to the reported issue. The sample was received with extension tubing. The sample received was functionally tested, the extension tube is part of the sample received was connected to a new 16 fr. Catheter (is not part of the sample received) after the sample was tested passing water through of new 16 fr. Catheter, and noted the liquid flow toward the interior of the bags until is filled to its maximum capacity. During this test, did not note that the flow stopped. The flow was continuous. At last, the liquid of the leg bags was drained to the exterior of the bags and did not note any difficulty or problem to drain. Additionally the vinyl? S were cut to verify the embossed of the bags to be correct on the sample received and no problem noted on the embossed. During the test of the sample received in the assembly extension tubing to bag not was observed problem of the leak in the assembly. After that, the bag was cut checked the embossed on the flutter valve on the sample received. Reviewed the inlet tube of the bag where the flutter valve is sealed for any type of obstruction and no problem was found. Reviewed that the flutter valve was not bend or had any type of obstruction and no problem was found. Reviewed the embossed of the flutter valve, which is on the external part; therefore, the assembly is correct. Reviewed the embossed of the clear vinyl of the leg bag, which is on the internal part; therefore, the assembly is correct. Reviewed the peripheral seal, rotary seal of the bags and no problem was found. No problem could be noticed on the flutter valve on the sample received the device history record was reviewed and found nothing that could have caused or contributed to the reported event. The instructions for use state the following: " position bag on leg with flutter valve at top. Attach catheter or extension tubing to top inlet. When wearing bag below knee, attach bard? Extension tubing (catalog no. 150615 or 4a4194). When using extension tubing, make sure to connect tube at least to the 3rd taper of the connector. To empty dispoz-a-bag? , push green lever on flip-flo? Valve out and down. " (b)(4). The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard.
Patient Sequence No: 1, Text Type: N, H10
[79163900]
It was reported that urine leaked into the inlet tube. Subsequently, urine would not flow into the tube.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1018233-2017-01642 |
| MDR Report Key | 6472709 |
| Date Received | 2017-04-07 |
| Date of Report | 2017-06-01 |
| Date Mfgr Received | 2017-05-08 |
| Date Added to Maude | 2017-04-07 |
| 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 |
| Reporter Occupation | OTHER CAREGIVERS |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | AMY GRAVLEY |
| Manufacturer Street | 8195 INDUSTRIAL BLVD |
| Manufacturer City | COVINGTON GA 30014 |
| Manufacturer Country | US |
| Manufacturer Postal | 30014 |
| Manufacturer Phone | 7707846100 |
| Manufacturer G1 | PRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590 |
| Manufacturer Street | KM. 7 CARRETERA INTERNACIONAL |
| Manufacturer City | NOGALES, SONORA 85621 |
| Manufacturer Country | MX |
| Manufacturer Postal Code | 85621 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BARD DISPOZ-A-BAG LEG BAG |
| Generic Name | LEG BAG |
| Product Code | FAQ |
| Date Received | 2017-04-07 |
| Returned To Mfg | 2017-04-04 |
| Catalog Number | UNK |
| Lot Number | UNK |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590 |
| Manufacturer Address | KM. 7 CARRETERA INTERNACIONAL NOGALES, SONORA 85621 MX 85621 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-04-07 |