Reported Sep 25, 2013 · Terminated

BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775 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?

  • BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture
  • Part Number72200775 Biodegradable suture anchor
Lot codes and dates
  • 50252371, 50252817, 50252818, 50253051, 50253556, 50254393, 50255140, 50255943, 50257230, 50257886, 50258390, 50258813, 50259145, 50259748, 50259820, 50260127, 50261934, 50263317, 50263909, 50264101, 50264417, 50264775, 50265257, 50265457, 50265935, 50266338, 50266709, 50266926, 50267287, 50267297, 50267742, 50268009, 50268284, 50268801, 50269502, 50269812, 50270227, 50270716, 50271271, 50271608, 50271908, 50272544, 50273015, 50273358, 50273640, 50273933, 50274557, 50274799, 50275368, 50276253, 50276254, 50276805, 50277029, 50277294, 50277527, 50277929, 50278456, 50278571, 50278899, 50279282, 50279628, 50279887, 50280270, 50280509, 50280951, 50281119, 50281654, 50281988, 50282538, 50282785, 50283315, 50283661, 50284261, 50284507, 50285047, 50285232, 50286292, 50286603, 50287484, 50287742, 50287951, 50288412, 50288413, 50288709, 50288711, 50289018, 50289361, 50289598, 50290037,50290863, 50291536, 50291656, 50292239, 50292240, 50292919, 50293285, 50293609, 50293897 50294168, 50294377, 50295055,

    231 of 231 codes

    • 50295263
    • 50296219
    • 50296742
    • 50297227
    • 50297778
    • 50297779
    • 50297780
    • 50298062
    • 50298419
    • 50298786
    • 50299246
    • 50299545
    • 50299546
    • 50299826
    • 50300216
    • 50300804
    • 50301267
    • 50301404
    • 50302151
    • 50302685
    • 50303058
    • 50303427
    • 50303788
    • 50303941
    • 50304178
    • 50304532
    • 50305224
    • 50305593
    • 50306159
    • 50306607
    • 50306999
    • 50307177
    • 50307178
    • 50307323
    • 50307855
    • 50308129
    • 50308350
    • 50308876
    • 50309006
    • 50309569
    • 50309929
    • 50310088
    • 50310360
    • 50310603
    • 50311024
    • 50311465
    • 50311593
    • 50312088
    • 50312508
    • 50312903
    • 50313096
    • 50313194
    • 50313433
    • 50313434
    • 50313810
    • 50313981
    • 50314087
    • 50314275
    • 50314383
    • 50314587
Amount recalled
43385 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.