MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2014-05-08 for CELSIOR manufactured by Genzyme Polyclonals S.a.s..
[4403889]
This unsolicited device case from united states was received on (b)(6) 2014 from a health care professional (other). This case was cross referenced with (b)(4) (cluster). This is a summary case of 05 patients who developed delayed graft function after undergoing heart transplantations which were preserved with celsior organ preservation solution (celsior). The medical history, past drugs, concurrent conditions and concomitant medications were not provided for all the patients. On unknown dates, the hearts for transplant were preserved in celsior organ preservation solution. On unknown dates, the patients underwent heart transplant. On unspecified dates, after unknown time frame, these patients had delayed graft function. Reportedly, they expected to have good outcomes but they did not. Corrective treatment: not reported. Outcome: unk. Seriousness criteria: important medical event (ime). A pharmaceutical technical complaint (ptc) was initiated and results were pending for the same.
Patient Sequence No: 1, Text Type: D, B5
[11871207]
Pharmacovigilance comment: sanofi company dated (b)(4) 2014: this case concerns a group of five patients who had delayed graft function after using celsior organ preservation solution for organ preservation. Although the role of the organ preservation solution cannot be ruled out based on the device event temporal relationship; however, lack of detailed information about medical history, lab data, any concurrent medical illnesses, clinical course etc. Of the patient precludes a comprehensive assessment in this case.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2950168-2014-58896 |
| MDR Report Key | 3827530 |
| Report Source | 05 |
| Date Received | 2014-05-08 |
| Date of Report | 2014-04-29 |
| Date Mfgr Received | 2014-04-29 |
| Date Added to Maude | 2014-05-23 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MICHAEL MURPHY |
| Manufacturer Street | 55 CORPORATE DR MAIL STOP: 55D-205A |
| Manufacturer City | BRIDGEWATER NJ 08807 |
| Manufacturer Country | US |
| Manufacturer Postal | 08807 |
| Manufacturer Phone | 9089813633 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CELSIOR |
| Generic Name | ORGAN PRESERVATION SOLUTION |
| Product Code | MSB |
| Date Received | 2014-05-08 |
| Lot Number | UNK |
| Operator | HEALTH PROFESSIONAL |
| Device Age | DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | GENZYME POLYCLONALS S.A.S. |
| Manufacturer Address | LYON |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2014-05-08 |