Aesculap Implant Systems LLC: Medical Device Recall in 2023 - (Recall #: Z-2146-2023)

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 Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610

Product Classification:

Class II

Date Initiated: May 18, 2023

Date Posted: July 26, 2023

Recall Number: Z-2146-2023

Event ID: 92575

Reason for Recall:

Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.

Status: Ongoing

Product Quantity: 7 units

Code Information:

GUIDID: 04046963469054 Lot Number: 22002834

Distribution Pattern:

US Nationwide distribution in the states of DC, MO, PA, TX.

Voluntary or Mandated:

Voluntary: Firm initiated