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 |