Drug recall
LITe Decompression Snake Arm, REF 48080230
FDA recall event 93573 · Class II · Stryker Spine
Key facts
| Event ID | 93573 |
|---|---|
| Recall numbers | Z-0610-2024 |
| Recalling firm | Stryker Spine |
| Product type | Devices |
| Products | LITe Decompression Snake Arm, REF 48080230 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft. |
| Initiation date | Nov 1, 2023 |
| Report date | Dec 27, 2023 |
| City | Allendale |
| State | NJ |
| Country | United States |
| FEI number | 3004024955 |
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: