Drug recall
Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for…
FDA recall event 92079 · Class II · Aesculap Implant Systems LLC
Key facts
| Event ID | 92079 |
|---|---|
| Recall numbers | Z-1569-2023 |
| Recalling firm | Aesculap Implant Systems LLC |
| Product type | Devices |
| Products | Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body. |
| Initiation date | Mar 21, 2023 |
| Report date | May 17, 2023 |
| 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: