Reported Sep 25, 2013 · Terminated

OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number: 72201994 Biodegradable suture…

Smith & Nephew, Inc. Endoscopy Division

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 Division · 150 Minuteman Drive · Andover, MA · 01810-1031

Is this the product you have?

  • OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue
  • Part Number72201994 Biodegradable suture anchor
Lot codes and dates
  • 129 of 129 codes

    • 50261490
    • 50270751
    • 50270752
    • 50272328
    • 50272465
    • 50274463
    • 50275816
    • 50277797
    • 50281885
    • 50282824
    • 50284636
    • 50286043
    • 50289368
    • 50294562
    • 50295821
    • 50299025
    • 50302162
    • 50307324
    • 50309971
    • 50315070
    • 50316291
    • 50318787
    • 50321649
    • 50323781
    • 50326576
    • 50327051
    • 50328246
    • 50329605
    • 50330164
    • 50330433
    • 50333202
    • 50333957
    • 50334241
    • 50335882
    • 50338130
    • 50338996
    • 50340050
    • 50340627
    • 50342110
    • 50344240
    • 50347147
    • 50348649
    • 50349265
    • 50352033
    • 50352702
    • 50354093
    • 50355668
    • 50356988
    • 50358386
    • 50358575
    • 50360455
    • 50361180
    • 50364371
    • 50364916
    • 50364917
    • 50367984
    • 50370095
    • 50370386
    • 50372674
    • 50372726
Amount recalled
6373 US

This recall covers 26 products

The agency filed one notice per product. You are reading one of them; the other 25 are below.

13 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 20, 2016 · Data as of Sep 19, 4:50 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.