Aesculap Implant Systems LLC: Medical Device Recall in 2023 - (Recall #: Z-1430-2023)

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:

Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only. A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments. Note: The CCR basket lid is also distributed with ME764 CCR Basket - Full System

Product Classification:

Class II

Date Initiated: February 23, 2023

Date Posted: May 3, 2023

Recall Number: Z-1430-2023

Event ID: 91968

Reason for Recall:

Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607.

Status: Ongoing

Product Quantity: ME754: 3 units; ME764: 22 units

Code Information:

GUIDID: 04046955299592 (Basket Lid)

Distribution Pattern:

US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX.

Voluntary or Mandated:

Voluntary: Firm initiated