MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-12-20 for PNEUMOCLEAR PLUS CO2 CONDITIONING INSUFFLATOR (AMERICAS) FM300 0620050000 manufactured by Stryker Endoscopy-san Jose.
[172224947]
Additional information will be provided once the investigation has been completed.
Patient Sequence No: 1, Text Type: N, H10
[172224948]
It was reported that the patient experienced slowed heart rate resulting in the need for medical intervention to return heart rate to normal.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0002936485-2019-00592 |
| MDR Report Key | 9500901 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2019-12-20 |
| Date of Report | 2020-03-10 |
| Date of Event | 2019-12-11 |
| Date Mfgr Received | 2019-12-11 |
| Device Manufacturer Date | 2019-07-01 |
| Date Added to Maude | 2019-12-20 |
| 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 | MR. CHESTER REBUGIO |
| Manufacturer Street | 5900 OPTICAL COURT |
| Manufacturer City | SAN JOSE CA 95138 |
| Manufacturer Country | US |
| Manufacturer Postal | 95138 |
| Manufacturer Phone | 4087542000 |
| Manufacturer G1 | STRYKER ENDOSCOPY-SAN JOSE |
| Manufacturer Street | 5900 OPTICAL COURT |
| Manufacturer City | SAN JOSE CA 95138 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 95138 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PNEUMOCLEAR PLUS CO2 CONDITIONING INSUFFLATOR (AMERICAS) |
| Generic Name | INSUFFLATOR, LAPAROSCOPIC |
| Product Code | HIF |
| Date Received | 2019-12-20 |
| Returned To Mfg | 2019-12-18 |
| Model Number | FM300 |
| Catalog Number | 0620050000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER ENDOSCOPY-SAN JOSE |
| Manufacturer Address | 5900 OPTICAL COURT SAN JOSE CA 95138 US 95138 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-12-20 |