Drug recall
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
FDA recall event 96732 · Class II · MEDLINE INDUSTRIES, LP - Northfield
Key facts
| Event ID | 96732 |
|---|---|
| Recall numbers | Z-1765-2025, Z-1766-2025 |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield |
| Product type | Devices |
| Products | Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395, Centurion Sterile Weitlaner Retractor, Reorder: 67315 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Three is the potential for the retractors to puncture through the sterile packaging. |
| Initiation date | Apr 9, 2025 |
| Report date | May 21, 2025 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
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: