MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-02-19 for POLAR CARE CUBE 10701 manufactured by Breg, Inc.
| Report Number | 2028253-2020-00001 |
| MDR Report Key | 9727684 |
| Report Source | OTHER |
| Date Received | 2020-02-19 |
| Date of Report | 2020-02-12 |
| Date Mfgr Received | 2020-01-20 |
| Date Added to Maude | 2020-02-19 |
| 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 | MRS. CAROL EMERSON |
| Manufacturer Street | 2885 LOKER AVENUE EAST |
| Manufacturer City | CARLSBAD, CA |
| Manufacturer Country | US |
| Manufacturer Phone | 7955823 |
| Manufacturer G1 | BREG, INC. |
| Manufacturer Street | 2885 LOKER AVENUE EAST |
| Manufacturer City | CARLSBAD, CA |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | POLAR CARE CUBE |
| Generic Name | POLAR CARE CUBE |
| Product Code | ILO |
| Date Received | 2020-02-19 |
| Model Number | 10701 |
| Catalog Number | 10701 |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BREG, INC |
| Manufacturer Address | 2885 LOKER AVENUE EAST CARLSBAD, CA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2020-02-19 |