Drug recall
Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref: A22020500
FDA recall event 84765 · Class II · Medicrea International
Key facts
| Event ID | 84765 |
|---|---|
| Recall numbers | Z-1234-2020 |
| Recalling firm | Medicrea International |
| Product type | Devices |
| Products | Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220) |
| Initiation date | Nov 11, 2019 |
| Report date | Feb 26, 2020 |
| Termination date | Oct 14, 2020 |
| 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: