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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-2216-2010 - Trabecular Metal acetabular revision system column buttress left posterior/right anterior, 00-4894-300-00, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address...
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2
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08/12/2010
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FEI # 1000220733 Zimmer Inc.
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Z-2217-2010 - Trabecular Metal acetabular revision system column buttress right posterior/left anterior, 00-4894-400-00, sterile, Zimmer Inc., Parsippany, NJ.
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2
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08/12/2010
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FEI # 1000220733 Zimmer Inc.
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Z-2215-2010 - Trabecular Metal acetabular revision system buttress augment size, 58, 00-4898-001-58, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address bony deficiencies o...
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2
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08/12/2010
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FEI # 1000220733 Zimmer Inc.
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Z-2214-2010 - Trabecular Metal acetabular revision system buttress augment size, 54, 00-4898-001-54, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address bony deficiencies o...
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2
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08/12/2010
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FEI # 1000220733 Zimmer Inc.
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