Reported Sep 25, 2013 · Terminated

OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue ; Part Number: 72201995 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 / Blue
  • Part Number72201995 Biodegradable suture anchor
Lot codes and dates
  • 160 of 160 codes

    • 50272329
    • 50272466
    • 50274208
    • 50274464
    • 50274790
    • 50275814
    • 50277799
    • 50278266
    • 50278994
    • 50282166
    • 50283019
    • 50283839
    • 50285057
    • 50286656
    • 50288421
    • 50289813
    • 50291359
    • 50293118
    • 50294563
    • 50295608
    • 50296649
    • 50298065
    • 50301017
    • 50302318
    • 50305467
    • 50306821
    • 50308347
    • 50309211
    • 50310089
    • 50310614
    • 50311296
    • 50312591
    • 50314389
    • 50315223
    • 50315419
    • 50316180
    • 50316679
    • 50316987
    • 50317481
    • 50318376
    • 50318532
    • 50319543
    • 50320363
    • 50321935
    • 50323084
    • 50323631
    • 50324184
    • 50324789
    • 50327218
    • 50331339
    • 50333094
    • 50336659
    • 50339177
    • 50340628
    • 50343607
    • 50345140
    • 50345975
    • 50347750
    • 50349688
    • 50352034
Amount recalled
17696 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, 5:38 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.