CER BIOLOXD MOD HD 36MM -3 NK Adverse Event — Injury (MDR 3002806535-2020-00232)
CER BIOLOXD MOD HD 36MM -3 NK Adverse Event — Injury (MDR 3002806535-2020-00232) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CER BIOLOXD MOD HD 36MM -3 NK; Generic name: HIP ARTHROPLASTY; Manufacturer: BIOMET UK LTD..
| Device | CER BIOLOXD MOD HD 36MM -3 NK |
|---|---|
| Generic name | HIP ARTHROPLASTY |
| Manufacturer | BIOMET UK LTD. |
| Report number | 3002806535-2020-00232 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | (B)(4). THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. THE FOLLOWING SECTIONS WERE UPDATED: B4, B5, G4, G7, H1, H2, H10. ADDITIONAL INFORMATION RECEIVED: -ON (B)(6) 2020, A SUPERFICIAL I&D WAS PERFORMED FOR WOUND DEHISCENCE. -THE OUTCOME IS PENDING. |
| Source | openFDA MAUDE (device adverse events) |
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