Aesculap Implant Systems LLC: Medical Device Recalls in 2023

According to to data from the FDA, there were 4 medical device recalls made by Aesculap Implant Systems LLC in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

• 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
• For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R
• 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
• Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610