Tornier, Inc: Medical Device Recall in 2015 - (Recall #: Z-2465-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Salto Talaris Tibial Guide, Part # MJU333 ,Tray/Kit Code YKAL11, Non sterile. Orthopedic Manual Surgical Instrument

Product Classification:

Class II

Date Initiated: August 6, 2015

Date Posted: September 2, 2015

Recall Number: Z-2465-2015

Event ID: 71913

Reason for Recall:

Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide (part number MJU333) due to a complaint that occurred during physician training, that the guide cannot be assembled to the Salto Talaris Talar Pin Setting guide. This issue will cause the impossibility the time of putting the Talar pin in the guide.

Status: Terminated

Product Quantity: 5

Code Information:

Lot #14F005

Distribution Pattern:

Distributed to CA, ME, NC, PA, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated