ENSEAL GENERIC PRODUCT CODE Adverse Event — Injury (MDR 3005075853-2020-02351)
ENSEAL GENERIC PRODUCT CODE Adverse Event — Injury (MDR 3005075853-2020-02351) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENSEAL GENERIC PRODUCT CODE; Generic name: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES; Manufacturer: ETHICON ENDO-SURGERY, LLC..
| Device | ENSEAL GENERIC PRODUCT CODE |
|---|---|
| Generic name | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Manufacturer | ETHICON ENDO-SURGERY, LLC. |
| Report number | 3005075853-2020-02351 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | FOREIGN, LITERATURE |
| Narrative | (B)(4). DATE SENT: 04/27/2020. DATE OF EVENT: UNKNOWN. BATCH # UNKNOWN. THIS REPORT IS RELATED TO A JOURNAL ARTICLE, THEREFORE NO PRODUCT WILL BE RETURNED FOR ANALYSIS AND THE BATCH HISTORY RECORDS CANNOT BE REVIEWED AS THE LOT/BATCH NUMBER HAS NOT BEEN PROVIDED. |
| Source | openFDA MAUDE (device adverse events) |
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