Reported Jan 13, 2021 · Terminated
Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft…
Smith & Nephew, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Smith & Nephew, Inc. · 1450 E Brooks Rd · Memphis, TN · 38116-1804
Is this the product you have?
- Bone fixation nail
- TRIGEN INTERTAN - Product Usageindicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fracture
- Lot codes and dates
- Model #: 71675535 & 71675532 Lot #: 20CM25278 & 20DM01466.
- Amount recalled
- 41 units
Where it was sold
Why it was recalled
Manufacturing packaging error.
This product could cause temporary or reversible health problems — stop using it.
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