Drug recall
Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
FDA recall event 80863 · Class II · Stryker GmbH
Key facts
| Event ID | 80863 |
|---|---|
| Recall numbers | Z-3240-2018 |
| Recalling firm | Stryker GmbH |
| Product type | Devices |
| Products | Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | When creating a correction plan with the Correct Axial First button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an erroneously… |
| Initiation date | Jul 26, 2018 |
| Report date | Oct 3, 2018 |
| Termination date | May 26, 2020 |
| City | Selzach |
| Country | Switzerland |
| FEI number | 3002807830 |
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: