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In2Bones, SAS recalls DUAFIT(R) PIP 0o CA SIZE 3, REF A60 SP003, STERILE R, Rx only. Interphalangeal implant.
Recalled April 1, 2015 · FDA recall Z-1319-2015 · In2Bones, SAS
Hazard
Dimensional non-conformity leading to the impossibility to introduce the implant in the dedicated holder. · FDA Class II
Units
15 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 3, REF A60 SP003, 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 →