Aesculap Implant Systems LLC: Medical Device Recall in 2023 - (Recall #: Z-2518-2023)

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:

For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R

Product Classification:

Class II

Date Initiated: July 20, 2023

Date Posted: September 13, 2023

Recall Number: Z-2518-2023

Event ID: 92813

Reason for Recall:

Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30¿ neuroendoscope, a portion of the visual field is obscured.

Status: Ongoing

Product Quantity: 25 units

Code Information:

UDI-DI: 04038653065547 Lot Numbers: 52750146 52753381, 52756472, 52768317, 52805655, 52812596, 52816570, 52823878, 52830872. Serial Numbers: 4281,4282, 4284,4288, 4289,4291, 4308,4309, 4310, 4312, 4313,4336, 4340,4341, 4342,4402, 4411, 4412, 4413,4414, 4422,4439, 4447,4449, 4450

Distribution Pattern:

US Nationwide distribution in the states of FL, ID, IL, MD, NC, NY, OR, RI, TX.

Voluntary or Mandated:

Voluntary: Firm initiated