Reported Sep 25, 2013 · Terminated

OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number: 72201993 Biodegradable suture anchor

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 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue
  • Part Number72201993 Biodegradable suture anchor
Lot codes and dates
  • 306 of 306 codes

    • 50261071
    • 50265227
    • 50268236
    • 50270124
    • 50270127
    • 50270731
    • 50270732
    • 50270944
    • 50272331
    • 50272463
    • 50272751
    • 50274143
    • 50274349
    • 50277106
    • 50278834
    • 50281659
    • 50282211
    • 50282825
    • 50283848
    • 50285062
    • 50287130
    • 50288422
    • 50289369
    • 50291056
    • 50292247
    • 50293722
    • 50295044
    • 50295954
    • 50297046
    • 50298435
    • 50299024
    • 50301146
    • 50301385
    • 50302078
    • 50306608
    • 50307181
    • 50307859
    • 50308888
    • 50308912
    • 50309137
    • 50311191
    • 50312587
    • 50314102
    • 50315238
    • 50316441
    • 50316664
    • 50317482
    • 50317875
    • 50318971
    • 50319908
    • 50320248
    • 50321101
    • 50321648
    • 50322088
    • 50322930
    • 50323639
    • 50324385
    • 50325610
    • 50325737
    • 50326879
Amount recalled
25733

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.