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Recall Observatory FDA recall evidence

Device product

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

Z-1319-2015

March 09, 2015

Class II

Product summary

Firm
In2Bones, SAS
Event
Event 70736
Status
Terminated
Classification
Class II
Quantity
15 units
Official record key
device-enforcement:Z-1319-2015

Official wording

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

Code information: Batch numbers: 1412021

Distribution pattern: Distributed in the state of TN.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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