Aesculap Implant Systems LLC: Medical Device Recall in 2012 - (Recall #: Z-2114-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant (SJ780T-US) Product Usage: The Aesculap Implant Systems SIBD Trial Implant instruments assist the surgeon in selecting the correct size implant for the patient

Product Classification:

Class II

Date Initiated: July 12, 2012

Date Posted: August 8, 2012

Recall Number: Z-2114-2012

Event ID: 62626

Reason for Recall:

The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are correctly dimensioned, but the part number etched on the instrument may be incorrect. The 4 degree trial instrument (SJ768T-US) may be marked with the incorrect part number of the 9 degree trail instrument (SJ780T-US) and the 9 degree trial instrument (SJ780T-US) may be marked with the incorrect part number of the 4 degree tria

Status: Terminated

Product Quantity: 5

Code Information:

4 degree - SJ768T-US and 9 degree SJ780T-US

Distribution Pattern:

US Nationwide Distribution - including the states of CO, OH, OK and TX.

Voluntary or Mandated:

Voluntary: Firm initiated