UNK VOLBELLA Adverse Event — Injury (MDR 3005113652-2020-00219)
UNK VOLBELLA Adverse Event — Injury (MDR 3005113652-2020-00219) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNK VOLBELLA; Generic name: IMPLANT, DERMAL, FOR AESTHETIC USE; Manufacturer: ALLERGAN (PRINGY).
| Device | UNK VOLBELLA |
|---|---|
| Generic name | IMPLANT, DERMAL, FOR AESTHETIC USE |
| Manufacturer | ALLERGAN (PRINGY) |
| Report number | 3005113652-2020-00219 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER, OTHER |
| Narrative | THIS MEDWATCH IS IN RESPONSE TO FDA REPORT NUMBER MW 5093524. NO CONTACT INFORMATION WAS PROVIDED FOR THE PATIENT, THEREFORE ADDITIONAL EVENT, PRODUCT, AND/OR PATIENT DETAILS ARE NOT ATTAINABLE. THE EVENT IS A PHYSIOLOGICAL COMPLICATION AND ANALYSIS OF THE DEVICE GENERALLY DOES NOT ASSIST ALLERGAN IN DETERMINING A PROBABLE CAUSE FOR THIS EVENT. THIS IS A KNOWN POTENTIAL ADVERSE EVENT ADDRESSED IN |
| Source | openFDA MAUDE (device adverse events) |
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