Reported Sep 25, 2013 · Terminated

OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black; Part Number: 72201996 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?

  • OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black
  • Part Number72201996 Biodegradable suture anchor
Lot codes and dates
  • 76 of 76 codes

    • 50272330
    • 50272467
    • 50274209
    • 50274465
    • 50274791
    • 50275815
    • 50277800
    • 50292667
    • 50296071
    • 50302316
    • 50306994
    • 50310605
    • 50311297
    • 50316179
    • 50318681
    • 50321243
    • 50323086
    • 50325048
    • 50325601
    • 50326880
    • 50329010
    • 50329811
    • 50334408
    • 50336660
    • 50338997
    • 50340629
    • 50344015
    • 50346092
    • 50346624
    • 50353156
    • 50354524
    • 50356989
    • 50358564
    • 50363890
    • 50364919
    • 50368628
    • 50370206
    • 50374882
    • 50376601
    • 50378711
    • 50381816
    • 50385513
    • 50390999
    • 50391628
    • 50392410
    • 50395539
    • 50400939
    • 50403274
    • 50404746
    • 50406677
    • 50408208
    • 50409818
    • 50412886
    • 50414333
    • 50415150
    • 50416320
    • 50417391
    • 50418417
    • 50419567
    • 50421499
Amount recalled
5873 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, 5:31 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.