Reported Oct 28, 2015 · Terminated

Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm, Sterile Part Number: 7209237 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 8.5 mm
  • Sterile Part Number7209237
  • Intended UseFor arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects
Lot codes and dates
  • 71 of 71 codes

    • 50069280
    • 50214249
    • 50260936
    • 50334160
    • 50380067
    • 50410625
    • 50442600
    • 50084563
    • 50217938
    • 50266144
    • 50337465
    • 50383809
    • 50412120
    • 50448621
    • 50097669
    • 50227860
    • 50276674
    • 50352665
    • 50385382
    • 50415177
    • 50451051
    • 50112174
    • 50231228
    • 50282533
    • 50353524
    • 50389835
    • 50416603
    • 50451744
    • 50117989
    • 50236270
    • 50310331
    • 50356943
    • 50391478
    • 50424410
    • 50452069
    • 50131406
    • 50242373
    • 50317889
    • 50362696
    • 50396029
    • 50428473
    • 50455380
    • 50139181
    • 50246739
    • 50320168
    • 50370396
    • 50399036
    • 50428686
    • 50457280
    • 50148410
    • 50254144
    • 50324084
    • 50372214
    • 50401621
    • 50432549
    • 50461109
    • 50199543
    • 50254145
    • 50328908
    • 50374300
Amount recalled
1246 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, 4:44 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.