Drug recall
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
FDA recall event 93856 · Class II · Aesculap Inc
Key facts
| Event ID | 93856 |
|---|---|
| Recall numbers | Z-1243-2024, Z-1244-2024, Z-1245-2024, Z-1246-2024, Z-1247-2024 |
| Recalling firm | Aesculap Inc |
| Product type | Devices |
| Products | DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures., DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures., DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures., DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures., DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The sterile blister packaging may be damaged, and sterility may be compromised. |
| Initiation date | Jan 9, 2024 |
| Report date | Mar 13, 2024 |
| City | Center Valley |
| State | PA |
| Country | United States |
| FEI number | 2916714 |
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: