Reported Apr 29, 2020 · Ongoing
Smith & Nephew FOOTPRINT Ultra PK Suture Anchor, 5.5mm Part Number: 72202902
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. · 130 & 120 Forbes Blvd · Mansfield, MA · 02048
Is this the product you have?
- Smith & Nephew FOOTPRINT Ultra PK Suture Anchor, 5.5mm
- Part Number72202902
- Lot codes and dates
- Lot Numbers
247 of 247 codes
201388920139162013955201429620161972016198201623220162332016234201739520177612017818201781920186392018801201885520198412019893201999220213272021390202139120214992022264202226520222662022267202480920250642025065202516520251692025343202538620273982027429202862020292512029252202925320292542029295202929620292972029298202933720293382029339202934020293862029387203093720309382030939203094020310772031078203107920310802031145
- Lot Numbers
- Amount recalled
- 125,196 (Total)
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
Space between the device and the packaging permits excessive movement which could potentially lead to the displacement of the anchor s tip protector allowing the tip of the anchor to create a sterile breach.
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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