MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-02-26 for VERRES NEEDLE manufactured by Ethicon Endo Surgery, Llc.
[3174823]
Verres needle would not push gas into abdominal cavity. Hose itself was working. Apparatus seemed blocked. No adverse event injury to the pt. Reason for use: laparoscopic low anterior resection.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5029199 |
| MDR Report Key | 2993125 |
| Date Received | 2013-02-26 |
| Date of Report | 2013-02-26 |
| Date of Event | 2012-11-20 |
| Date Added to Maude | 2013-03-08 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VERRES NEEDLE |
| Generic Name | VERRES NEEDLE |
| Product Code | FHO |
| Date Received | 2013-02-26 |
| Lot Number | J4CE99 |
| Device Expiration Date | 2017-08-29 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ETHICON ENDO SURGERY, LLC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-02-26 |