Reported Aug 19, 2020 · Ongoing
Tibial knee prosthesis
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?
- Tibial knee prosthesis
- Lot codes and dates
- Model
7142016471420166
- and 71420184 Lot Numbers
128 of 128 codes
19MT3145719MT3145819MT3145920AT3261120AT3261220AT3261320AT3354020AT3354120AT3354220AT3354320AT3354420AT3354520AT3354620AT3354720AT3354820AT3356920AT3357020AT3357120BT3385620BT3385720BT3385820BT3385920BT3386020BT3386120BT3386220BT3386320BT3386420BT3386520BT3386620BT3387820BT3387920BT3388020BT3388120BT3388220BT3388320BT3388420BT3388520BT3388620BT3388720BT3388820BT3388920BT3435720BT3435820BT3435920BT3436020BT3437920BT3438020BT3438120BT3438220BT3438320BT3438420BT3438520BT34386H2008427G1923903G1923904G1923905G1923933G1923934G1923935
- Model
- Amount recalled
- 1,845 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Due to an inconsistency in the raw material process, specific lots may contain units with internal non-homogenous material defects.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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