Drug recall
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
FDA recall event 84770 · Class II · Medicrea International
Key facts
| Event ID | 84770 |
|---|---|
| Recall numbers | Z-1156-2020 |
| Recalling firm | Medicrea International |
| Product type | Devices |
| Products | Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter |
| Initiation date | Oct 2, 2019 |
| Report date | Feb 19, 2020 |
| Termination date | Feb 8, 2021 |
| City | Rillieux La Pape |
| Country | France |
| FEI number | 1000432246 |
At a glance
- 1–9 Products in this recall
- 1–9 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: