MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-23 for BARD MEDICAL manufactured by Bard Medical.
[101029205]
Post-operative patient ordered for discharge. Surgeon ordered removal of drain - rn attempted to remove drain with gentle traction. Drain broke in half and remaining drain left inside the patient. Surgeon consulted general surgery and patient returned to surgery for drain removal. Return to surgery (b)(6) 2017.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5075519 |
| MDR Report Key | 7295982 |
| Date Received | 2018-02-23 |
| Date of Report | 2018-02-22 |
| Date of Event | 2017-12-26 |
| Date Added to Maude | 2018-02-26 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | BARD MEDICAL |
| Generic Name | WOUND DRAIN RELIAVAC |
| Product Code | GCD |
| Date Received | 2018-02-23 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BARD MEDICAL |
| Manufacturer Address | COVINGTON GA 30014 US 30014 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-02-23 |