Reported Oct 28, 2015 · Terminated

Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm, Sterile Part Number: 7209236 Intended Use: For…

Smith & Nephew, Inc., Endoscopy Div.

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., Endoscopy Div. · 130 Forbes Blvd · Mansfield, MA · 02048

Is this the product you have?

  • Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm
  • Sterile Part Number7209236
  • Intended UseFor arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects
Lot codes and dates
  • 82 of 82 codes

    • 567531
    • 50182767
    • 50242031
    • 50311086
    • 50354626
    • 50396028
    • 50419909
    • 50451050
    • 50481583
    • 586717
    • 50193108
    • 50251239
    • 50311900
    • 50361147
    • 50400191
    • 50423797
    • 50451742
    • L50195027
    • 50023445
    • 50195027
    • 50254749
    • 50322127
    • 50372399
    • 50402518
    • 50427083
    • 50452777
    • 50031093
    • 50200477
    • 50257710
    • 50326789
    • 50375128
    • 50404802
    • 50431408
    • 50455222
    • 50089906
    • 50207485
    • 50260093
    • 50331945
    • 50376693
    • 50405482
    • 50432856
    • 50456255
    • 50112893
    • 50214248
    • 50266143
    • 50337081
    • 50379780
    • 50408076
    • 50433676
    • 50460255
    • 50129647
    • 50218992
    • 50279513
    • 50337265
    • 50381258
    • 50408437
    • 50442599
    • 50469461
    • 50160551
    • 50221872
Amount recalled
1347 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Sterility of device is compromised due to breach in the packaging

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 23, 2021 · Data as of Sep 19, 6:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.