Aesculap Implant Systems LLC: Medical Device Recall in 2023 - (Recall #: Z-1569-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery. Product Code: PL771SU

Product Classification:

Class II

Date Initiated: March 21, 2023

Date Posted: May 17, 2023

Recall Number: Z-1569-2023

Event ID: 92079

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.

Status: Ongoing

Product Quantity: 6 pieces

Code Information:

UDI-DI: 04046964837340 Lot Number: 52785146

Distribution Pattern:

US Nationwide distribution in the state of OH.

Voluntary or Mandated:

Voluntary: Firm initiated