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U.S. Department of Health and Human Services

Medical Device Recalls
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181 to 190 of 500 Results *
Recall Date to: 11/27/2015
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Product Description
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FDA Recall
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T2 3.5x130mm AO Drill Bit 2 02/26/2003 Stryker Howmedica Osteonics
Gamma Drill Dia. 4.2x300mm 2 02/26/2003 Stryker Howmedica Osteonics
Gamma AO Drill 5.5x300mm 2 02/26/2003 Stryker Howmedica Osteonics
Modular femoral and proximal tibial replacement system consisting of femoral head/neck, body, stem a... 2 02/27/2003 Stryker Howmedica Osteonics
Modular Replacement System with Extra-Cortical Porous Coating, Femoral Module Stem and Tibial Module... 2 02/27/2003 Stryker Howmedica Osteonics
Scimed PT Graphix Intermediate PCTA Guide Wire with ICE Hydrophilic Coating, 300 cm length. 3 02/27/2003 Symbiosis Corp.
Scimed ChoICE PT Extra Support PTCA Guide Wire with ICE Hydrophilic Coating, 300 cm length 3 02/27/2003 Symbiosis Corp.
MultiDiagnost 4 - x-ray system, multi functional/universal system for general use. 2 02/27/2003 Philips Medical Systems
Product is a ChoICE 182 cm Guide Wire, intended to facilitate placement of balloon dilatation cathet... 3 02/27/2003 Symbiosis Corp.
Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device packaged in a carri... 3 02/27/2003 Symbiosis Corp.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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