Encore Medical, Lp: Medical Device Recall in 2017 - (Recall #: Z-3102-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

MODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers: REF S-200956 - 5mm PIN, SIZE 46 REF S-200957 - 5mm PIN, SIZE 50 REF S-200958 - 5mm PIN, SIZE 58

Product Classification:

Class II

Date Initiated: August 4, 2017

Date Posted: September 6, 2017

Recall Number: Z-3102-2017

Event ID: 77930

Reason for Recall:

It was reported that the models used to manufacture S-200956/958 had the wrong dimension used to create the spherical radius cutting surface. Device design allows a larger spherical radius cutting surface than intended.

Status: Terminated

Product Quantity: 5 units

Code Information:

Catalog number, Lot Number S-200956, 535U1000 S-200957, 536U1000 S-200958, 537U1000

Distribution Pattern:

OH, VA

Voluntary or Mandated:

Voluntary: Firm initiated