Aesculap Implant Systems LLC: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Aesculap Implant Systems LLC in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.