Reported Apr 29, 2020 · Ongoing
Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901
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 4.5
- Part Number72202901
- Lot codes and dates
- Lot Numbers
437 of 437 codes
201202020120212012022201382220138232013887201388820139142013915201395420168012017394201739720174012017759201776020177632017764201776820177712017815201781620178172017846201784720178482017849201863820187422018799201880020188532019892201999120200522021389202149820215462023225202327320232742023336202333720247622024764202480620248082025068202507020251572025160202516320252902025291202534220265612027397202742820274602028121
- 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 anchors 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.
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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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