MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-06-11 for ENDO CLINCH II 174317 manufactured by Us Surgical Puerto Rico.
[110620428]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[110620429]
According to the reporter, while they were grasping tissue to hold it in place in a laparoscopic procedure, one side of the grasping jaws detached and fell into the abdomen. They also noted that the handles were unable to bind. They removed the jaw piece by using another grasping device. They opened a new device with the same lot number to complete the case. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5
[119673314]
Additional information: evaluation summary: post market vigilance (pmv) led an evaluation of six devices. The actual device used was not evaluated, returned devices were all sealed. No abnormalities were found during visual inspection and functional testing of the returned product. Records from each manufacturing lot are thoroughly reviewed to ensure that products are released meeting all quality release specifications at the time of manufacture. Analysis concluded there were no assembly component related failures. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[119673315]
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2647580-2018-02808 |
| MDR Report Key | 7587195 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2018-06-11 |
| Date of Report | 2018-09-06 |
| Date of Event | 2018-04-17 |
| Date Mfgr Received | 2018-08-20 |
| Device Manufacturer Date | 2017-08-07 |
| Date Added to Maude | 2018-06-11 |
| 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 | 3 |
| Manufacturer Contact | LISA HERNANDEZ |
| Manufacturer Street | 60 MIDDLETOWN AVE |
| Manufacturer City | NORTH HAVEN CT 06473 |
| Manufacturer Country | US |
| Manufacturer Postal | 06473 |
| Manufacturer Phone | 2034925563 |
| Manufacturer G1 | US SURGICAL PUERTO RICO |
| Manufacturer Street | 201 SABANETAS INDUSTRIAL PARK |
| Manufacturer City | PONCE PR 007164401 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 007164401 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ENDO CLINCH II |
| Generic Name | FORCEPS, OBSTETRICAL |
| Product Code | HDA |
| Date Received | 2018-06-11 |
| Returned To Mfg | 2018-06-26 |
| Model Number | 174317 |
| Catalog Number | 174317 |
| Lot Number | P7H1365PX |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | US SURGICAL PUERTO RICO |
| Manufacturer Address | 201 SABANETAS INDUSTRIAL PARK PONCE PR 007164401 US 007164401 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-06-11 |