Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DUAFIT(R) PIP 0o CA SIZE 3 Recalled by In2Bones, SAS Due to Dimensional non-conformity leading to the impossibility to introduce...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact In2Bones, SAS directly.
Affected Products
DUAFIT(R) PIP 0o CA SIZE 3, REF A60 SP003, STERILE R, Rx only. Interphalangeal implant.
Quantity: 15 units
Why Was This Recalled?
Dimensional non-conformity leading to the impossibility to introduce the implant in the dedicated holder.
Where Was This Sold?
This product was distributed to 1 state: TN
About In2Bones, SAS
In2Bones, SAS has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report