MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2020-03-25 for VERSAPORT PLUS 179103P manufactured by Davis & Geck Caribe Ltd.
        [185497298]
If information is provided in the future, a supplemental report will be issued.
 Patient Sequence No: 1, Text Type: N, H10
        [185497299]
According to the reporter, during procedure, the plug part of the device came off. Another device was used to complete the case. There was no patient injury.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9612501-2020-00521 | 
| MDR Report Key | 9879540 | 
| Report Source | FOREIGN,USER FACILITY | 
| Date Received | 2020-03-25 | 
| Date of Report | 2020-03-25 | 
| Date of Event | 2020-03-06 | 
| Date Mfgr Received | 2020-03-06 | 
| Device Manufacturer Date | 2019-07-02 | 
| Date Added to Maude | 2020-03-25 | 
| 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 | DAVIS & GECK CARIBE LTD | 
| Manufacturer Street | ZONA FRANCA DE SAN ISIDRO | 
| Manufacturer City | SANTO DOMINGO 0101 | 
| Manufacturer Country | DO | 
| Manufacturer Postal Code | 0101 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | VERSAPORT PLUS | 
| Generic Name | LAPAROSCOPE, GENERAL & PLASTIC SURGERY | 
| Product Code | GCJ | 
| Date Received | 2020-03-25 | 
| Model Number | 179103P | 
| Catalog Number | 179103P | 
| Lot Number | J9G0244Y | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | * | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | DAVIS & GECK CARIBE LTD | 
| Manufacturer Address | ZONA FRANCA DE SAN ISIDRO SANTO DOMINGO 0101 DO 0101 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2020-03-25 |