Legion(tm) Hemi Step Tibial Wedge Rk/hk recall
LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432 Product Usage: The constrained knee systems are designed for use…
Why was Legion(tm) Hemi Step Tibial Wedge Rk/hk recalled?
The affected products were inadvertently packaged with an incorrect screw component.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
13KSL0038C
- Product
- LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432 Product Usage: The constrained knee systems are designed for use…
- Recalling firm
- Smith & Nephew, Inc.
- Quantity
- 12 units
- Distribution
- Foreign countries of; France, Germany, Netherlands, Norway, Switzerland
- Recall date
- September 18, 2019
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)