Reported Sep 25, 2013 · Terminated

OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black; Part Number: 72201992 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 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black
  • Part Number72201992 Biodegradable suture anchor
Lot codes and dates
  • 195 of 195 codes

    • 50272332
    • 50272462
    • 50272750
    • 50274144
    • 50274350
    • 50277105
    • 50278907
    • 50281510
    • 50282171
    • 50282827
    • 50283849
    • 50284637
    • 50285830
    • 50286658
    • 50287767
    • 50289371
    • 50290043
    • 50291934
    • 50292091
    • 50295383
    • 50296070
    • 50297228
    • 50297782
    • 50298793
    • 50300135
    • 50301932
    • 50306856
    • 50307462
    • 50308037
    • 50309210
    • 50310436
    • 50310780
    • 50312090
    • 50313439
    • 50313818
    • 50314915
    • 50315807
    • 50316601
    • 50316986
    • 50317483
    • 50318001
    • 50318687
    • 50319907
    • 50320679
    • 50321916
    • 50322244
    • 50323257
    • 50323630
    • 50323780
    • 50324608
    • 50325611
    • 50326067
    • 50327821
    • 50329242
    • 50331546
    • 50332253
    • 50333092
    • 50334400
    • 50335620
    • 50336405
Amount recalled
18919

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, 6:50 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.