Reported Jun 17, 2026 · Ongoing

NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic…

In2bones USA, LLC

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: In2bones USA, LLC · 7750a Trinity Rd · Cordova, TN · 38018-2722

Is this the product you have?

  • NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 10x10x10 UDI-DI Code00817906020083 T50 SN012 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 12x12x12 UDI-DI Code00817906020090 T50 SN020 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 20x20x20 UDI-DI Code00817906020151 T50 SN110 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 10x15x13 UDI-DI Code00817906020113 T50 SN115 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 15Wx15x15 UDI-DI Code00817906020137 T50 SN118 NeoSpan¿ SuperElastic Compression Staple w/Instruments
  • Size 18x14x14 UDI-DI Code00810021861364 Single/multiple component metallic bone fixation appliances and accessories The In2Bones USA NeoSpan" Compression Staple Implant w/instruments is indicated for hand and foot bone fragments, osteotomy fixation and joint arthrodesis
Lot codes and dates
  • Catalog No. Lot Code
    • T50
    • SN010
    • 1962242
    • 1964665
    • 2054541
    • 2039361
    • T50
    • SN012
    • 1963511
    • T50
    • SN020
    • 1971252
    • 1990642
    • 2027441
    • T50
    • SN110
    • 1971241
    • T50
    • SN115
    • 19647210
    • T50
    • SN118
    • 1990631
Amount recalled
306 kits

Where it was sold

Why it was recalled

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

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

Data as of Sep 19, 3:41 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.