In2Bones, SAS: Medical Device Recall in 2015 - (Recall #: Z-1319-2015)

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:

DUAFIT(R) PIP 0o CA SIZE 3, REF A60 SP003, STERILE R, Rx only. Interphalangeal implant.

Product Classification:

Class II

Date Initiated: March 9, 2015

Date Posted: April 1, 2015

Recall Number: Z-1319-2015

Event ID: 70736

Reason for Recall:

Dimensional non-conformity leading to the impossibility to introduce the implant in the dedicated holder.

Status: Terminated

Product Quantity: 15 units

Code Information:

Batch numbers: 1412021

Distribution Pattern:

Distributed in the state of TN.

Voluntary or Mandated:

Voluntary: Firm initiated