Drug recall
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
FDA recall event 82973 · Class II · Ethicon Endo-Surgery Inc
Key facts
| Event ID | 82973 |
|---|---|
| Recall numbers | Z-1888-2019, Z-1889-2019, Z-1890-2019 |
| Recalling firm | Ethicon Endo-Surgery Inc |
| Product type | Devices |
| Products | Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C, Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C, Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Observed reported incidence rate for harm associated with intraoperative bleeding |
| Initiation date | May 15, 2019 |
| Report date | Jul 3, 2019 |
| Termination date | Jun 11, 2020 |
| City | Blue Ash |
| State | OH |
| Country | United States |
| FEI number | 1527736 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: