Drug recall
Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product…
FDA recall event 98282 · Class II · Centinel Spine, Inc.
Key facts
| Event ID | 98282 |
|---|---|
| Recall numbers | Z-1426-2026 |
| Recalling firm | Centinel Spine, Inc. |
| Product type | Devices |
| Products | Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Products were mislabeled as the 6mm product but included the 5 mm product. |
| Initiation date | Dec 31, 2025 |
| Report date | Feb 25, 2026 |
| City | West Chester |
| State | PA |
| Country | United States |
| FEI number | 3007494564 |
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: