RecallWatchUSA

Home / Recalls / Medical Devices

In2Bones, SAS recalls DUAFIT(R) PIP 0o CA SIZE 2, REF A60 SP002, STERILE R, Rx only. Interphalangeal implant.

Recalled April 1, 2015 · FDA recall Z-1318-2015 · In2Bones, SAS

Hazard
Dimensional non-conformity leading to the impossibility to introduce the implant in the dedicated holder. · FDA Class II
Units
35 units
Sold at
Distributed in the state of TN.

Description

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

Product
DUAFIT(R) PIP 0o CA SIZE 2, REF A60 SP002, STERILE R, Rx only. Interphalangeal implant.
Manufacturer(s)
In2Bones, SAS
Made in
France

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

In2Bones, SAS recalls DUAFIT(R) PIP 0o CA SIZE 2, REF A60 SP002, STERILE R, Rx only. Interphalangeal implant. | RecallWatchUSA