Aesculap Implant Systems LLC: Medical Device Recall in 2019 - (Recall #: Z-2496-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: August 7, 2019

Date Posted: September 18, 2019

Recall Number: Z-2496-2019

Event ID: 83637

Reason for Recall:

possibility of the sterility batch being insufficiently sterilized

Status: Terminated

Product Quantity: 3 unit of Lot 837B

Code Information:

Lot # 109C and 837B

Distribution Pattern:

US Nationwide distribution in the state of CA.

Voluntary or Mandated:

Voluntary: Firm initiated