MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-01-08 for BELZER UW COLD STORAGE SOLUTION manufactured by Preservation Solutions, Inc..
[96665377]
Preservation solutions inc, (psi, manufacturer) received information from (b)(4) on july 24, 2017 via email that (b)(4) had received a complaint regarding belzer uw cold storage solution. The initial information provided to psi indicates that (b)(6) medical center ((b)(6), user) in spokane, washington knowingly used belzer uw cold storage solution off-label on a heart transplant. Post-operation, there was difficulty restarting the heart. Psi contacted (b)(6) via the email provided by (b)(4) on july 26, 2017 with a list of questions regarding the complaint. (b)(6) contacted psi by phone on july 28, 2017 and insinuated that the questions would be answered in the coming days. During the phone call, psi discovered that there were two patients, one female and one male (form 3500a filed separately) experiencing complications after under going heart transplants. Both heart transplants knowingly used the belzer uw cold storage solution off-label. As of (b)(6) 2017, the female patient was experiencing right ventricle/pulmonary problems and was in a medically induced coma. (b)(6) indicated that both hearts came from the same donor hospital. Psi has been unable to obtain any additional information, or answers to the questions asked, from (b)(6) since the july 28, 2017 phone conversation. All psi inquiries for information and answers to the questions have been met with generalized responses stating that the questions have been answered but are currently undergoing review by (b)(6). Psi will continue to follow-up with (b)(6) as part of its investigation.
Patient Sequence No: 1, Text Type: N, H10
[96665378]
Preservation solutions inc, (psi, manufacturer) received information from (b)(4) on july 24, 2017 via email that (b)(4) had received a complaint regarding belzer uw cold storage solution. The initial information provided to psi indicates that (b)(6) medical center ((b)(6), user) in (b)(6) knowingly used belzer uw cold storage solution off-label on a heart transplant. Post-operation, there was difficulty restarting the heart. Psi contacted (b)(6) via the email provided by (b)(4) on july 26, 2017 with a list of questions regarding the complaint. (b)(6) contacted psi by phone on july 28, 2017 and insinuated that the questions would be answered in the coming days. During the phone call, psi discovered that there were two patients, one female and one male (form 3500a filed separately) experiencing complications after under going heart transplants. Both heart transplants knowingly used the belzer uw cold storage solution off-label. As of (b)(6) 2017, the female patient was experiencing right ventricle/pulmonary problems and was in a medically induced coma. (b)(6) indicated that both hearts came from the same donor hospital. Psi has been unable to obtain any additional information, or answers to the questions asked, from (b)(6) since the july 28, 2017 phone conversation. All psi inquiries for information and answers to the questions have been met with generalized responses stating that the questions have been answered but are currently undergoing review by (b)(6). Psi will continue to follow-up with (b)(6) as part of its investigation. No new relevant information as of january 5, 2018.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1000221028-2017-00084 |
| MDR Report Key | 7173059 |
| Report Source | DISTRIBUTOR |
| Date Received | 2018-01-08 |
| Date of Report | 2017-09-01 |
| Date Mfgr Received | 2017-07-24 |
| Date Added to Maude | 2018-01-08 |
| 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 | SCOTT FISHER |
| Manufacturer Street | 1099 PROCTOR DRIVE |
| Manufacturer City | ELKHORN WI 53121 |
| Manufacturer Country | US |
| Manufacturer Postal | 53121 |
| Manufacturer Phone | 2627236715 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BELZER UW COLD STORAGE SOLUTION |
| Generic Name | BELZER UW COLD STORAGE SOLUTION |
| Product Code | KDN |
| Date Received | 2018-01-08 |
| Device Availability | * |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PRESERVATION SOLUTIONS, INC. |
| Manufacturer Address | 1099 PROCTOR DRIVE ELKHORN WI 53121 US 53121 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Other; 4. Required No Informationntervention | 2018-01-08 |