Reported Oct 28, 2015 · Terminated

Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 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 4.5 mm
  • Sterile Part Number7209235
  • Intended UseFor arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects
Lot codes and dates
  • 62 of 62 codes

    • 50051865
    • 50218987
    • 50317627
    • 50353758
    • 50405160
    • 50451743
    • 50481584
    • 50067670
    • 50230666
    • 50322491
    • 50361146
    • 50408123
    • 50452778
    • S603582
    • 50081261
    • 50234894
    • 50329870
    • 50372414
    • 50411652
    • 50455378
    • 50120770
    • 50238931
    • 50331389
    • 50376694
    • 50415117
    • 50456676
    • 50121527
    • 50242557
    • 50335918
    • 50379781
    • 50418789
    • 50458024
    • 50180302
    • 50248824
    • 50337463
    • 50381854
    • 50419542
    • 50460414
    • 50194727
    • 50253762
    • 50340709
    • 50383822
    • 50419729
    • 50462250
    • 50204111
    • 50257419
    • 50340713
    • 50387833
    • 50427066
    • 50465245
    • 50207090
    • 50277081
    • 50345713
    • 50390055
    • 50428661
    • 50476968
    • 50209127
    • 50285673
    • 50348084
    • 50395389
Amount recalled
1287 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.